folic acid

Generic: folic acid

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name folic acid
Generic Name folic acid
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

folic acid 1 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7224
Product ID 0904-7224_2b0b349c-5d44-4f5b-89c7-d56afdc92f98
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040625
Listing Expiration 2026-12-31
Marketing Start 2022-03-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047224
Hyphenated Format 0904-7224

Supplemental Identifiers

RxCUI
310410
UNII
935E97BOY8

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name folic acid (source: ndc)
Generic Name folic acid (source: ndc)
Application Number ANDA040625 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7224-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7224-61 100 BLISTER PACK in 1 CARTON (0904-7224-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

folic acid (1 mg/1)

Linked Drug Pages (1)

Folic Acid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b0b349c-5d44-4f5b-89c7-d56afdc92f98", "openfda": {"unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["7778ac96-7817-455a-a177-22ecb276c67f"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7224-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7224-61", "marketing_start_date": "20220621"}], "brand_name": "Folic Acid", "product_id": "0904-7224_2b0b349c-5d44-4f5b-89c7-d56afdc92f98", "dosage_form": "TABLET", "product_ndc": "0904-7224", "generic_name": "Folic Acid", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Folic Acid", "active_ingredients": [{"name": "FOLIC ACID", "strength": "1 mg/1"}], "application_number": "ANDA040625", "marketing_category": "ANDA", "marketing_start_date": "20220307", "listing_expiration_date": "20261231"}