Is Kesin Pharma Corporation FDA approved?

Kesin Pharma Corporation holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Kesin Pharma Corporation's registered sites?

The FDA register lists Oldsmar, FL. Registered operations: labelling, packaging, repackaging.

What drugs does Kesin Pharma Corporation make?

45 products are listed under Kesin Pharma Corporation in the openFDA NDC Directory, most often as solution; suspension; liquid. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Kesin Pharma Corporation

Data as of 28 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 45
Labeller names: 4
Live patents: 0
Countries: 1
Base: United States

Authorisation

Registered operations

Labelling1Packaging1Repackaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Kesin Pharma Corporation	3874 Tampa Rd Ste 103,, Oldsmar, Florida (FL) 34677-3126, United States (USA)	Labelling, Packaging, Repackaging	3016965788117447816

Catalogue

Drug listings by form and route

45 active NDC listings: 29 human prescription drug, 16 human otc drug. By marketing category: ANDA 28, OTC MONOGRAPH DRUG 12, UNAPPROVED DRUG OTHER 4, NDA 1.

Dosage form	NDCs
solution	20
suspension	13
liquid	3
powder, for solution	2
tablet	2
elixir	1
granule, for solution	1
ointment	1
powder, for suspension	1
syrup	1

Route	NDCs
oral	43
dental	1
rectal	1
topical	1

Labeller name on the listing	NDCs
kesin pharma corporation	36
kesin pharma	6
kesin pharma corporation	2
kesin pharmaceutical corporation	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Atovaquone	Atovaquone	suspension, oral	81033-104ANDA
Atovaquone Oral Suspension	Atovaquone	suspension, oral	81033-105ANDA
CHILDRENS Acetaminophen	CHILDRENS Acetaminophen	suspension, oral	81033-026OTC MONOGRAPH DRUG
CHILDRENS Ibuprofen	Ibuprofen	suspension, oral	81033-019ANDA
Chlorhexidine Gluconate, 0.12% Oral Rinse Solution	Chlorhexidine Gluconate, 0.12% Oral Rinse	solution, dental	81033-512ANDA
Dexamethasone	Dexamethasone	elixir, oral	81033-010ANDA
Dextromethorphan HBr and Guaifenesin Oral Solution	Dextromethorphan HBr and Guaifenesin Oral Solution	liquid, oral	81033-103OTC MONOGRAPH DRUG
Diphenhydramine HCl Oral Solution	Diphenhydramine HCl Oral Solution	solution, oral	81033-029OTC MONOGRAPH DRUG
Docusate Sodium Oral Liquid	Docusate Sodium Oral Liquid	liquid, oral	81033-022OTC MONOGRAPH DRUG
FAMOTIDINE	FAMOTIDINE	powder, for suspension, oral	81033-023ANDA
Fosfomycin Tromethamine	Fosfomycin Tromethamine	granule, for solution, oral	81033-024ANDA
Gabapentin	Gabapentin	solution, oral	81033-123ANDA
Gabapentin	Gabapentin	solution, oral	81033-124ANDA
Guaifenesin	Guaifenesin	liquid, oral	81033-102OTC MONOGRAPH DRUG
Hydroxyzine Hydrochloride	Hydroxyzine Hydrochloride	solution, oral	81033-031ANDA
Kesin MAG-AL	Aluminum and Magnesium Hydroxide Suspension	suspension, oral	81033-005OTC MONOGRAPH DRUG
Kesin MAG-AL Plus	Aluminum and Magnesium Hydroxide w/Simethicone Suspension	suspension, oral	81033-006OTC MONOGRAPH DRUG
Kesin MAG-AL Plus XS	Aluminum and Magnesium Hydroxide w/Simethicone Suspension	suspension, oral	81033-007OTC MONOGRAPH DRUG
LEVETIRACETAM	LEVETIRACETAM	solution, oral	81033-013ANDA
LIKMEZ	Metronidazole Oral	suspension, oral	81033-066NDA
Lacosamide Oral Solution	Lacosamide	solution, oral	81033-427ANDA
Lacosamide Oral Solution	Lacosamide	solution, oral	81033-428ANDA
Lactulose Solution	Lactulose Solution USP, 10 g/15 mL	solution, oral, rectal	81033-241ANDA
Loperamide Hydrochloride	Loperamide Hydrochloride	solution, oral	81033-067ANDA
Magnesium Oxide	Magnesium Oxide	tablet, oral	81033-027OTC MONOGRAPH DRUG
Megestrol Acetate	Megestrol Acetate	suspension, oral	81033-150ANDA
Milk of Magnesia	Magnesium Hydroxide	suspension, oral	81033-014OTC MONOGRAPH DRUG
Mineral Oil	Mineral Oil	solution, oral	81033-042OTC MONOGRAPH DRUG
Mupirocin	Mupirocin Ointment	ointment, topical	81033-032ANDA
NYSTATIN	NYSTATIN	suspension, oral	81033-015ANDA
POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	solution, oral	81033-220ANDA
POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	solution, oral	81033-240ANDA
PROMETHAZINE HYDROCHLORIDE	PROMETHAZINE HYDROCHLORIDE	solution, oral	81033-016ANDA
Phenobarbital Oral Solution	Phenobarbital Oral	solution, oral	81033-163UNAPPROVED DRUG OTHER
Phenobarbital Oral Solution	Phenobarbital Oral	solution, oral	81033-164UNAPPROVED DRUG OTHER
Polyethylene Glycol 3350	Polyethylene Glycol 3350	powder, for solution, oral	81033-762ANDA
Potassium Chloride	Potassium Chloride	powder, for solution, oral	81033-413ANDA
Senna Syrup	Senna Syrup	syrup, oral	81033-120OTC MONOGRAPH DRUG
Sodium Chloride	Sodium Chloride Tablets	tablet, oral	81033-028UNAPPROVED DRUG OTHER
Sodium Citrate and Citric Acid	Sodium Citrate and Citric Acid	solution, oral	81033-017UNAPPROVED DRUG OTHER
Sucralfate	Sucralfate	suspension, oral	81033-149ANDA
Sulfamethoxazole and Trimethoprim	Sulfamethoxazole and Trimethoprim	suspension, oral	81033-012ANDA
TOPIRAMATE	TOPIRAMATE	solution, oral	81033-035ANDA
Valproic Acid	Valproic Acid	solution, oral	81033-266ANDA
prednisoLONE sodium phosphate	prednisoLONE sodium phosphate	solution, oral	81033-021ANDA

Neighbours

Registered in the same town

Eagle Pharmaceuticals, Inc.Oldsmar, FL

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Enquiry

Common questions

Is Kesin Pharma Corporation FDA approved?: Kesin Pharma Corporation holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Kesin Pharma Corporation's registered sites?: The FDA register lists Oldsmar, FL. Registered operations: labelling, packaging, repackaging.
What drugs does Kesin Pharma Corporation make?: 45 products are listed under Kesin Pharma Corporation in the openFDA NDC Directory, most often as solution; suspension; liquid. 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.