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Last Updated: March 26, 2026

Details for New Drug Application (NDA): 211064

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NDA 211064 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. Thirty suppliers are listed for this compound. Additional details are available on the folic acid profile page.

Summary for 211064

Tradename:	FOLIC ACID
Applicant:	Rising
Ingredient:	folic acid
Patents:	0

Medical Subject Heading (MeSH) Categories for 211064

Hematinics
Vitamin B Complex

Suppliers and Packaging for NDA: 211064

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
FOLIC ACID	folic acid	TABLET;ORAL	211064	ANDA	Rising Pharma Holdings, Inc.	16571-881	16571-881-01	100 TABLET in 1 BOTTLE (16571-881-01)
FOLIC ACID	folic acid	TABLET;ORAL	211064	ANDA	Rising Pharma Holdings, Inc.	16571-881	16571-881-10	1000 TABLET in 1 BOTTLE (16571-881-10)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	1MG
Approval Date:	Mar 8, 2019	TE:	AA	RLD:	No

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