folic acid

Generic: folic acid

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name folic acid
Generic Name folic acid
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

folic acid 1 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-004
Product ID 82868-004_46dc8b44-bf33-8a68-e063-6394a90a5ae9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040625
Listing Expiration 2026-12-31
Marketing Start 2023-08-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82868004
Hyphenated Format 82868-004

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
  • 30 TABLET in 1 BOTTLE, PLASTIC (82868-004-30)
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": "46dc8b44-bf33-8a68-e063-6394a90a5ae9", "openfda": {"unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["03b0aee4-804a-de63-e063-6394a90a6635"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-004-30)", "package_ndc": "82868-004-30", "marketing_start_date": "20230815"}], "brand_name": "Folic Acid", "product_id": "82868-004_46dc8b44-bf33-8a68-e063-6394a90a5ae9", "dosage_form": "TABLET", "product_ndc": "82868-004", "generic_name": "Folic Acid", "labeler_name": "Northwind Health Company, LLC", "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": "20230815", "listing_expiration_date": "20261231"}