Folic Acid

Product NDC
71335-9628
11-digit product format
713359628
Labeler code
71335
Product ID
71335-9628_e7614988-7196-4419-b0ce-9be637e38721
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Folic Acid
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA211064
Marketing category
ANDA
Marketing start
2022-10-25
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
71335-9628-17133596280130 TABLET in 1 BOTTLE (71335-9628-1) 30 tablet2023-01-17NoNoHistorical
71335-9628-271335962802100 TABLET in 1 BOTTLE (71335-9628-2) 100 tablet2023-01-17NoNoHistorical
71335-9628-371335962803120 TABLET in 1 BOTTLE (71335-9628-3) 120 tablet2023-01-17NoNoHistorical
71335-9628-47133596280450 TABLET in 1 BOTTLE (71335-9628-4) 50 tablet2023-01-17NoNoHistorical
71335-9628-57133596280590 TABLET in 1 BOTTLE (71335-9628-5) 90 tablet2023-01-17NoNoHistorical
71335-9628-67133596280660 TABLET in 1 BOTTLE (71335-9628-6) 60 tablet2023-01-17NoNoHistorical
71335-9628-77133596280710 TABLET in 1 BOTTLE (71335-9628-7) 10 tablet2023-01-17NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Folic Acid Tablets, USPBryant Ranch Prepack2024-08-23HUMAN PRESCRIPTION DRUG LABEL102