Is TAGI Pharma, Inc. FDA approved?

TAGI Pharma, Inc. holds no registered establishment of its own; 15 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does TAGI Pharma, Inc. make?

15 products are listed under TAGI Pharma, Inc. in the openFDA NDC Directory, most often as tablet; tablet, film coated; capsule. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

TAGI Pharma, Inc.

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

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Registered sites: 0
Active NDC listings: 15
Labeller names: 2
Live patents: 0
Countries: 0

Catalogue

Drug listings by form and route

15 active NDC listings: 15 human prescription drug. By marketing category: ANDA 15.

Dosage form	NDCs
tablet	3
tablet, film coated	3
capsule	2
powder, for suspension	2
tablet, coated	2
tablet, extended release	2
injection, solution, concentrate	1

Route	NDCs
oral	14
intravenous	1

Labeller name on the listing	NDCs
tagi pharma, inc.	14
tagi pharma inc.	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Azithromycin Dihydrate	Azithromycin Dihydrate	tablet, film coated, oral	51224-022ANDA
Azithromycin Dihydrate	Azithromycin Dihydrate	tablet, film coated, oral	51224-122ANDA
Benzonatate	Benzonatate	capsule, oral	51224-001ANDA
Benzonatate	Benzonatate	capsule, oral	51224-010ANDA
Chlorthalidone	Chlorthalidone	tablet, oral	51224-018ANDA
Chlorthalidone	Chlorthalidone	tablet, oral	51224-118ANDA
Cholestyramine	Cholestyramine	powder, for suspension, oral	51224-011ANDA
Cholestyramine Light	Cholestyramine	powder, for suspension, oral	51224-009ANDA
Gabapentin	Gabapentin	tablet, coated, oral	51224-021ANDA
Gabapentin	Gabapentin	tablet, coated, oral	51224-121ANDA
Levetiracetam	levetiracetam	injection, solution, concentrate, intravenous	51224-013ANDA
Metformin Hydrochloride	Metformin Hydrochloride	tablet, extended release, oral	51224-007ANDA
Metformin Hydrochloride	Metformin Hydrochloride	tablet, extended release, oral	51224-107ANDA
Naltrexone Hydrochloride	Naltrexone Hydrochloride	tablet, film coated, oral	51224-206ANDA
Phentermine Hydrochloride	Phentermine Hydrochloride	tablet, oral	51224-101ANDA

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Enquiry

Common questions

Is TAGI Pharma, Inc. FDA approved?: TAGI Pharma, Inc. holds no registered establishment of its own; 15 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does TAGI Pharma, Inc. make?: 15 products are listed under TAGI Pharma, Inc. in the openFDA NDC Directory, most often as tablet; tablet, film coated; capsule. 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.