Folic Acid

Product NDC
71335-2849
11-digit product format
713352849
Labeler code
71335
Product ID
71335-2849_588a56ed-e8d0-48b3-84ff-db18a211fa1e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Folic Acid
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA211064
Marketing category
ANDA
Marketing start
2018-02-09
Substance
FOLIC ACID
Active strength
1 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
935E97BOY8FOLIC ACID59-30-3FOLIC ACID

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2849-17133528490130 TABLET in 1 BOTTLE (71335-2849-1) 30 tablet2025-10-22NoNoHistorical
71335-2849-271335284902100 TABLET in 1 BOTTLE (71335-2849-2) 100 tablet2025-10-22NoNoHistorical
71335-2849-371335284903120 TABLET in 1 BOTTLE (71335-2849-3) 120 tablet2025-10-22NoNoHistorical
71335-2849-47133528490450 TABLET in 1 BOTTLE (71335-2849-4) 50 tablet2025-10-22NoNoHistorical
71335-2849-57133528490590 TABLET in 1 BOTTLE (71335-2849-5) 90 tablet2025-10-22NoNoHistorical
71335-2849-67133528490660 TABLET in 1 BOTTLE (71335-2849-6) 60 tablet2025-10-22NoNoHistorical
71335-2849-77133528490710 TABLET in 1 BOTTLE (71335-2849-7) 10 tablet2025-10-22NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Folic AcidBryant Ranch Prepack2025-10-22HUMAN PRESCRIPTION DRUG LABEL1