Folic Acid

Product NDC
68788-8827
11-digit product format
687888827
Labeler code
68788
Product ID
68788-8827_a4fd896d-0a44-4e53-bbb0-d716765e58b1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Folic Acid
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA202437
Marketing category
ANDA
Marketing start
2025-02-13
Substance
FOLIC ACID
Active strength
1 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data

Finished product
Yes
Brand name base
Folic Acid
Listing expiration
2026-12-31

Related Records

Active Ingredients

IngredientStrength
FOLIC ACID1 mg/1

Harmonized Identifiers

FieldValues
Unii935E97BOY8
Rxcui310410

Related Records

Related UNII Ingredients

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

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68788-8827-168788882701100 TABLET in 1 BOTTLE (68788-8827-1) 100 tablet2025-02-13NoNoHistorical
68788-8827-36878888270330 TABLET in 1 BOTTLE (68788-8827-3) 30 tablet2025-02-13NoNoHistorical
68788-8827-66878888270660 TABLET in 1 BOTTLE (68788-8827-6) 60 tablet2025-02-13NoNoHistorical
68788-8827-96878888270990 TABLET in 1 BOTTLE (68788-8827-9) 90 tablet2025-02-13NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rx onlyPreferred Pharmaceuticals Inc.2025-02-13HUMAN PRESCRIPTION DRUG LABEL1