folic acid

Generic: folic acid

Labeler: method pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name folic acid
Generic Name folic acid
Labeler method pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

folic acid 1 mg/1

Manufacturer
Method Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 58657-151
Product ID 58657-151_41b4d71d-2dc2-36bd-e063-6294a90af1e1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211064
Listing Expiration 2026-12-31
Marketing Start 2018-02-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58657151
Hyphenated Format 58657-151

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 ANDA211064 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (58657-151-01)
  • 1000 TABLET in 1 BOTTLE (58657-151-10)
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": "41b4d71d-2dc2-36bd-e063-6294a90af1e1", "openfda": {"unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["b9c315ff-cecb-8b75-e053-2995a90aa204"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58657-151-01)", "package_ndc": "58657-151-01", "marketing_start_date": "20210125"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (58657-151-10)", "package_ndc": "58657-151-10", "marketing_start_date": "20210125"}], "brand_name": "Folic Acid", "product_id": "58657-151_41b4d71d-2dc2-36bd-e063-6294a90af1e1", "dosage_form": "TABLET", "product_ndc": "58657-151", "generic_name": "Folic Acid", "labeler_name": "Method Pharmaceuticals, LLC", "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": "20180209", "listing_expiration_date": "20261231"}