Is BioComp Pharma, Inc. FDA approved?

BioComp Pharma, Inc. holds no registered establishment of its own; 28 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does BioComp Pharma, Inc. make?

28 products are listed under BioComp Pharma, Inc. in the openFDA NDC Directory, most often as cream; lotion; emulsion. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

BioComp Pharma, Inc.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 0
Active NDC listings: 28
Labeller names: 2
Live patents: 0
Countries: 0

Catalogue

Drug listings by form and route

28 active NDC listings: 28 human prescription drug. By marketing category: UNAPPROVED DRUG OTHER 19, NDA AUTHORIZED GENERIC 6, ANDA 3.

Dosage form	NDCs
cream	6
lotion	4
emulsion	3
liquid	3
tablet	3
solution	2
suspension	2
tablet, delayed release	2
shampoo	1
tablet, film coated	1
tablet, sugar coated	1

Route	NDCs
topical	19
oral	9

Labeller name on the listing	NDCs
biocomp pharma, inc.	25
biocomp pharma, inc.	3

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Carbinoxamine Maleate	Carbinoxamine Maleate	tablet, oral	44523-825ANDA
Gabapentin	Gabapentin	solution, oral	44523-120ANDA
Potassium Citrate	potassium citrate	tablet, oral	44523-410NDA AUTHORIZED GENERIC
Potassium Citrate	potassium citrate	tablet, oral	44523-415NDA AUTHORIZED GENERIC
Prednisolone Sodium Phosphate Oral Solution	Prednisolone Sodium Phosphate	solution, oral	44523-182ANDA
SODIUM SULFACETAMIDE	SODIUM SULFACETAMIDE	liquid, topical	44523-606UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE	SODIUM SULFACETAMIDE	liquid, topical	44523-613UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE AND SULFUR	SULFACETAMIDE SODIUM, SULFUR	lotion, topical	44523-600UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE AND SULFUR	SULFACETAMIDE SODIUM, SULFUR	lotion, topical	44523-602UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE AND SULFUR	SULFACETAMIDE SODIUM, SULFUR	cream, topical	44523-603UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE AND SULFUR	sodium sulfacetamide, sulfur	lotion, topical	44523-605UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE AND SULFUR	SULFACETAMIDE SODIUM, SULFUR	lotion, topical	44523-607UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE AND SULFUR	SULFACETAMIDE SODIUM, SULFUR	suspension, topical	44523-624UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE AND SULFUR	Sodium Sulfacetamide 9.8% and Sulfur 4.8%	emulsion, topical	44523-748UNAPPROVED DRUG OTHER
SODIUM SULFACETAMIDE, SULFUR	sulfacetamide sodium, sulfur	suspension, topical	44523-604UNAPPROVED DRUG OTHER
SULFACETAMIDE SODIUM	SULFACETAMIDE SODIUM	liquid, topical	44523-568UNAPPROVED DRUG OTHER
SULFACETAMIDE SODIUM, SULFUR	SULFACETAMIDE SODIUM, SULFUR	emulsion, topical	44523-560UNAPPROVED DRUG OTHER
Sodium Sulfacetamide	Sodium Sulfacetamide	shampoo, topical	44523-510UNAPPROVED DRUG OTHER
Sodium Sulfacetamide, Sulfur	SULFACETAMIDE SODIUM, SULFUR	cream, topical	44523-520UNAPPROVED DRUG OTHER
Sodium Sulfacetamide, Sulfur	SULFACETAMIDE SODIUM	cream, topical	44523-542UNAPPROVED DRUG OTHER
Sodium Sulfacetamide, Sulfur	SULFACETAMIDE SODIUM, SULFUR	emulsion, topical	44523-550UNAPPROVED DRUG OTHER
Tinidazole	tinidazole	tablet, film coated, oral	44523-450NDA AUTHORIZED GENERIC
Tiopronin	Tiopronin	tablet, sugar coated, oral	44523-053NDA AUTHORIZED GENERIC
Tiopronin	Tiopronin	tablet, delayed release, oral	44523-054NDA AUTHORIZED GENERIC
Tiopronin	Tiopronin	tablet, delayed release, oral	44523-055NDA AUTHORIZED GENERIC
UREA	UREA	cream, topical	44523-617UNAPPROVED DRUG OTHER
UREA	UREA	cream, topical	44523-618UNAPPROVED DRUG OTHER
Urea 39% Cream	Urea 39% Cream	cream, topical	44523-801UNAPPROVED DRUG OTHER

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Enquiry

Common questions

Is BioComp Pharma, Inc. FDA approved?: BioComp Pharma, Inc. holds no registered establishment of its own; 28 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does BioComp Pharma, Inc. make?: 28 products are listed under BioComp Pharma, Inc. in the openFDA NDC Directory, most often as cream; lotion; emulsion. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.