Fla. Stat. 499.041
Schedule of fees for drug, device, and cosmetic applications and permits, product registrations, and free-sale certificates


(1)

The department shall assess applicants requiring a manufacturing permit an annual fee within the ranges established in this section for the specific type of manufacturer.The fee for a prescription drug manufacturer permit may not be less than $500 or more than $750 annually.The fee for a device manufacturer permit may not be less than $500 or more than $600 annually.The fee for a cosmetic manufacturer permit shall be sufficient to cover the costs of administering the cosmetic manufacturer permit program.The fee for an over-the-counter drug manufacturer permit may not be less than $300 or more than $400 annually.The fee for a prescription drug repackager permit may not be less than $500 or more than $750 annually.A manufacturer may not be required to pay more than one fee per establishment to obtain an additional manufacturing permit, but each manufacturer must pay the highest fee applicable to his or her operation in each establishment.

(a)

The fee for a prescription drug manufacturer permit may not be less than $500 or more than $750 annually.

(b)

The fee for a device manufacturer permit may not be less than $500 or more than $600 annually.

(c)

The fee for a cosmetic manufacturer permit shall be sufficient to cover the costs of administering the cosmetic manufacturer permit program.

(d)

The fee for an over-the-counter drug manufacturer permit may not be less than $300 or more than $400 annually.

(e)

The fee for a prescription drug repackager permit may not be less than $500 or more than $750 annually.

(f)

A manufacturer may not be required to pay more than one fee per establishment to obtain an additional manufacturing permit, but each manufacturer must pay the highest fee applicable to his or her operation in each establishment.

(2)

The department shall assess an applicant that is required to have a wholesaling permit an annual fee within the ranges established in this section for the specific type of wholesaling.The fee for a prescription drug wholesale distributor permit may not be less than $300 or more than $800 annually.The fee for an out-of-state prescription drug wholesale distributor permit may not be less than $300 or more than $800 annually.The fee for a nonresident prescription drug manufacturer permit may not be less than $300 or more than $500 annually.The fee for a retail pharmacy drug wholesale distributor permit may not be less than $35 or more than $50 annually.The fee for a freight forwarder permit may not be less than $200 or more than $300 annually.The fee for a veterinary prescription drug wholesale distributor permit may not be less than $300 or more than $500 annually.The fee for a limited prescription drug veterinary wholesale distributor permit may not be less than $300 or more than $500 annually.The fee for a third party logistics provider permit may not be less than $200 or more than $300 annually.

(a)

The fee for a prescription drug wholesale distributor permit may not be less than $300 or more than $800 annually.

(b)

The fee for an out-of-state prescription drug wholesale distributor permit may not be less than $300 or more than $800 annually.

(c)

The fee for a nonresident prescription drug manufacturer permit may not be less than $300 or more than $500 annually.

(d)

The fee for a retail pharmacy drug wholesale distributor permit may not be less than $35 or more than $50 annually.

(e)

The fee for a freight forwarder permit may not be less than $200 or more than $300 annually.

(f)

The fee for a veterinary prescription drug wholesale distributor permit may not be less than $300 or more than $500 annually.

(g)

The fee for a limited prescription drug veterinary wholesale distributor permit may not be less than $300 or more than $500 annually.

(h)

The fee for a third party logistics provider permit may not be less than $200 or more than $300 annually.

(3)

The department shall assess an applicant that is required to have a retail establishment permit an annual fee within the ranges established in this section for the specific type of retail establishment.The fee for a veterinary prescription drug retail establishment permit may not be less than $200 or more than $300 annually.The fee for a health care clinic establishment permit may not be less than $125 or more than $250 annually.

(a)

The fee for a veterinary prescription drug retail establishment permit may not be less than $200 or more than $300 annually.

(b)

The fee for a health care clinic establishment permit may not be less than $125 or more than $250 annually.

(4)

The department shall assess an applicant that is required to have a restricted prescription drug distributor permit an annual fee of not less than $200 or more than $300.

(5)

In addition to the fee charged for a permit required by this part, the department shall assess applicants an initial application fee of $150 for each new permit issued by the department which requires an onsite inspection.

(6)

A person that is required to register drugs or devices under s. 499.015 shall pay an annual product registration fee of not less than $5 or more than $15 for each separate and distinct product in package form. The registration fee is in addition to the fee charged for a free-sale certificate.

(7)

The department shall assess an applicant that requests a free-sale certificate a fee of $25. A fee of $2 will be charged for each signature copy of a free-sale certificate that is obtained at the same time the free-sale certificate is issued.

(8)

The department shall assess an out-of-state prescription drug wholesale distributor applicant or permittee an onsite inspection fee of not less than $1,000 or more than $3,000 annually, to be based on the actual cost of the inspection if an onsite inspection is performed by agents of the department.

(9)

The department shall assess each person applying for certification as a designated representative a fee of $150, plus the cost of processing the criminal history record check.

(10)

The department shall assess other fees as provided in this part.

Source: Section 499.041 — Schedule of fees for drug, device, and cosmetic applications and permits, product registrations, and free-sale certificates, https://www.­flsenate.­gov/Laws/Statutes/2024/0499.­041 (accessed Aug. 7, 2025).

499.01
Permits
499.001
Florida Drug and Cosmetic Act
499.002
Purpose, administration, and enforcement of and exemption from this part
499.03
Possession of certain drugs without prescriptions unlawful
499.003
Definitions of terms used in this part
499.04
Fee authority
499.05
Rules
499.005
Prohibited acts
499.06
Embargoing, detaining, or destroying article or processing equipment which is in violation of law or rule
499.006
Adulterated drug or device
499.007
Misbranded drug or device
499.008
Adulterated cosmetics
499.009
Misbranded cosmetics
499.012
Permit application requirements
499.015
Registration of drugs and devices
499.023
New drugs
499.024
Drug product classification
499.025
Drug products in finished, solid, oral dosage form
499.026
Notification of manufacturer prescription drug price increases
499.028
Drug samples or complimentary drugs
499.029
Cancer Drug Donation Program
499.032
Phenylalanine
499.033
Ephedrine
499.035
Dimethyl sulfoxide (DMSO)
499.036
Restrictions on sale of dextromethorphan
499.039
Sale, distribution, or transfer of harmful chemical substances
499.041
Schedule of fees for drug, device, and cosmetic applications and permits, product registrations, and free-sale certificates
499.051
Inspections and investigations
499.0051
Criminal acts
499.052
Records of interstate shipment
499.0054
Advertising and labeling of drugs, devices, and cosmetics
499.055
Reports and dissemination of information by department
499.057
Expenses and salaries
499.062
Seizure and condemnation of drugs, devices, or cosmetics
499.065
Inspections
499.066
Penalties
499.067
Denial, suspension, or revocation of permit, certification, or registration
499.0121
Storage and handling of prescription drugs
499.0285
International Prescription Drug Importation Program
499.0295
Experimental treatments for terminal conditions
499.0661
Cease and desist orders
499.01201
Agency for Health Care Administration review and use of statute and rule violation or compliance data
499.01211
Drug Wholesale Distributor Advisory Council
499.02851
Federal arrangement to operate a pilot program for importing prescription drugs

Current through Fall 2025

§ 499.041. Schedule of fees for drug, device, & cosmetic applications and permits, product registrations, and free-sale certificates's source at flsenate​.gov