Is First Nation Group, LLC FDA approved?

First Nation Group, LLC holds no registered establishment of its own; 19 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does First Nation Group, LLC make?

19 products are listed under First Nation Group, LLC in the openFDA NDC Directory, most often as tablet; capsule; solution/ drops. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

First Nation Group, LLC

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

Request a quote Claim this profile

Registered sites: 0
Active NDC listings: 19
Labeller names: 2
Live patents: 0
Countries: 0

Catalogue

Drug listings by form and route

19 active NDC listings: 17 human prescription drug, 2 human otc drug. By marketing category: ANDA 18, OTC MONOGRAPH DRUG 1.

Dosage form	NDCs
tablet	7
capsule	5
solution/ drops	5
capsule, coated pellets	1
powder, for solution	1

Route	NDCs
oral	13
ophthalmic	5
topical	1

Labeller name on the listing	NDCs
first nation group, llc	18
first nation group	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Astringent Solution	Aluminum Sulfate Tetradecahydrate, Calcium Acetate Monohydrate	powder, for solution, topical	81469-999OTC MONOGRAPH DRUG
Bimatoprost	Bimatoprost	solution/ drops, ophthalmic	81469-291ANDA
Bumetanide	Bumetanide	tablet, oral	81469-221ANDA
Bumetanide	Bumetanide	tablet, oral	81469-222ANDA
Bumetanide	Bumetanide	tablet, oral	81469-223ANDA
Cetirizine Hydrochloride	Cetirizine Hydrochloride	tablet, oral	81469-353ANDA
Doxepin Hydrochloride	doxepin hydrochloride	capsule, oral	81469-415ANDA
Doxepin Hydrochloride	doxepin hydrochloride	capsule, oral	81469-416ANDA
Doxepin Hydrochloride	doxepin hydrochloride	capsule, oral	81469-417ANDA
Doxepin Hydrochloride	doxepin hydrochloride	capsule, oral	81469-418ANDA
Doxepin Hydrochloride	doxepin hydrochloride	capsule, oral	81469-419ANDA
Midodrine Hydrochloride	Midodrine Hydrochloride	tablet, oral	81469-139ANDA
Midodrine Hydrochloride	Midodrine Hydrochloride	tablet, oral	81469-140ANDA
Midodrine Hydrochloride	Midodrine Hydrochloride	tablet, oral	81469-141ANDA
Phenylephrine Hydrochloride	Phenylephrine Hydrochloride	solution/ drops, ophthalmic	81469-168ANDA
Phenylephrine Hydrochloride	Phenylephrine Hydrochloride	solution/ drops, ophthalmic	81469-169ANDA
divalproex sodium	divalproex sodium	capsule, coated pellets, oral	81469-492ANDA
timolol maleate	timolol maleate	solution/ drops, ophthalmic	81469-209ANDA
timolol maleate	timolol maleate	solution/ drops, ophthalmic	81469-210ANDA

Compare

Other companies listing doxepin hydrochloride

Patheon Manufacturing Services LLC19 sites · 319 NDC
Sun Pharmaceutical Industries Limited13 sites · 918 NDC
Teva Pharmaceutical Industries Ltd.6 sites · 668 NDC
Strides Pharma Science Limited5 sites · 230 NDC
Safecor Health, LLC3 sites · 103 NDC
Bryant Ranch Prepack1 site · 4,357 NDC
RemedyRepack, Inc1 site · 1,521 NDC
PD-Rx Pharmaceuticals Inc.1 site · 828 NDC
Golden State Medical Supply Inc.1 site · 670 NDC
Boswell Pharmacy Services LLC1 site · 15 NDC

Enquiry

Common questions

Is First Nation Group, LLC FDA approved?: First Nation Group, LLC holds no registered establishment of its own; 19 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does First Nation Group, LLC make?: 19 products are listed under First Nation Group, LLC in the openFDA NDC Directory, most often as tablet; capsule; solution/ drops. 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.