folic acid

Generic: folic acid

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name folic acid
Generic Name folic acid
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

folic acid 1 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2992
Product ID 68071-2992_2d53e5de-628b-12e9-e063-6294a90a6792
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211064
Listing Expiration 2026-12-31
Marketing Start 2022-10-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712992
Hyphenated Format 68071-2992

Supplemental Identifiers

RxCUI
310410
UPC
0368071299212
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 ANDA211064 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68071-2992-1)
source: ndc

Packages (1)

Ingredients (1)

folic acid (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d53e5de-628b-12e9-e063-6294a90a6792", "openfda": {"upc": ["0368071299212"], "unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["fa43f66c-9ae4-cd36-e053-6394a90a1526"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-2992-1)", "package_ndc": "68071-2992-1", "marketing_start_date": "20230426"}], "brand_name": "Folic Acid", "product_id": "68071-2992_2d53e5de-628b-12e9-e063-6294a90a6792", "dosage_form": "TABLET", "product_ndc": "68071-2992", "generic_name": "Folic Acid", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Folic Acid", "active_ingredients": [{"name": "FOLIC ACID", "strength": "1 mg/1"}], "application_number": "ANDA211064", "marketing_category": "ANDA", "marketing_start_date": "20221025", "listing_expiration_date": "20261231"}