Folic Acid

Product NDC
71335-2547
11-digit product format
713352547
Labeler code
71335
Product ID
71335-2547_b55fa556-0793-465c-9d62-2f21ff5331b5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Folic Acid
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA202437
Marketing category
ANDA
Marketing start
2018-11-20
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
71335-2547-17133525470130 TABLET in 1 BOTTLE (71335-2547-1) 30 tablet2025-01-21NoNoHistorical
71335-2547-271335254702100 TABLET in 1 BOTTLE (71335-2547-2) 100 tablet2025-01-21NoNoHistorical
71335-2547-371335254703120 TABLET in 1 BOTTLE (71335-2547-3) 120 tablet2025-01-21NoNoHistorical
71335-2547-47133525470450 TABLET in 1 BOTTLE (71335-2547-4) 50 tablet2025-01-21NoNoHistorical
71335-2547-57133525470590 TABLET in 1 BOTTLE (71335-2547-5) 90 tablet2025-01-21NoNoHistorical
71335-2547-67133525470660 TABLET in 1 BOTTLE (71335-2547-6) 60 tablet2025-01-21NoNoHistorical
71335-2547-77133525470710 TABLET in 1 BOTTLE (71335-2547-7) 10 tablet2025-01-21NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rx onlyBryant Ranch Prepack2025-01-21HUMAN PRESCRIPTION DRUG LABEL1