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Last Updated: December 12, 2025

Details for New Drug Application (NDA): 202437

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NDA 202437 describes FOLIC ACID, which is a drug marketed by Ben Venue, Fresenius Kabi Usa, Xgen Pharms, Aiping Pharm Inc, Amneal Pharm, Barr, Cadila Pharms Ltd, Chartwell Molecular, Contract Pharmacal, Everylife, Halsey, Hikma Pharms, Impax Labs, Ivax Sub Teva Pharms, Jubilant Cadista, Lannett, Leading, Lilly, Mk Labs, Nexgen Pharma Inc, Nuvo Pharms Inc, Ph Health, Pharmeral, Pioneer Pharms, Purepac Pharm, Rising, Sandoz, Sun Pharm Industries, Tablicaps, UDL, Usl Pharma, Valeant Pharm Intl, Vangard, Vintage Pharms, Watson Labs, and Whiteworth Town Plsn, and is included in thirty-eight NDAs. It is available from twenty-eight suppliers. Additional details are available on the FOLIC ACID profile page.

The generic ingredient in FOLIC ACID is folic acid. There are ten drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the folic acid profile page.

Summary for 202437

Tradename:	FOLIC ACID
Applicant:	Cadila Pharms Ltd
Ingredient:	folic acid
Patents:	0

Medical Subject Heading (MeSH) Categories for 202437

Hematinics
Vitamin B Complex

Suppliers and Packaging for NDA: 202437

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
FOLIC ACID	folic acid	TABLET;ORAL	202437	ANDA	Coupler LLC	67046-1449	67046-1449-3	30 TABLET in 1 BLISTER PACK (67046-1449-3)
FOLIC ACID	folic acid	TABLET;ORAL	202437	ANDA	Preferred Pharmaceuticals Inc.	68788-8827	68788-8827-1	100 TABLET in 1 BOTTLE (68788-8827-1)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	1MG
Approval Date:	Jan 27, 2014	TE:	AA	RLD:	No

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