folic acid

Generic: folic acid

Labeler: leading pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name folic acid
Generic Name folic acid
Labeler leading pharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

folic acid 1 mg/1

Manufacturer
Leading Pharma, LLC

Identifiers & Regulatory

Product NDC 69315-127
Product ID 69315-127_92322e52-3179-4738-8c8a-14fef62311d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040796
Listing Expiration 2026-12-31
Marketing Start 2009-01-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69315127
Hyphenated Format 69315-127

Supplemental Identifiers

RxCUI
310410
UNII
935E97BOY8

Packaging Origin

Original Packager
true

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 ANDA040796 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69315-127-01)
  • 1000 TABLET in 1 BOTTLE (69315-127-10)
source: ndc

Packages (2)

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": "92322e52-3179-4738-8c8a-14fef62311d4", "openfda": {"unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["1ba8c407-9613-4319-ac40-0a429cb0f3f4"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69315-127-01)", "package_ndc": "69315-127-01", "marketing_start_date": "20180221"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69315-127-10)", "package_ndc": "69315-127-10", "marketing_start_date": "20180221"}], "brand_name": "FOLIC ACID", "product_id": "69315-127_92322e52-3179-4738-8c8a-14fef62311d4", "dosage_form": "TABLET", "product_ndc": "69315-127", "generic_name": "FOLIC ACID", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FOLIC ACID", "active_ingredients": [{"name": "FOLIC ACID", "strength": "1 mg/1"}], "application_number": "ANDA040796", "marketing_category": "ANDA", "marketing_start_date": "20090112", "listing_expiration_date": "20261231"}