folic acid

Generic: folic acid

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

folic acid 1 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-791
Product ID 43063-791_303d4c3e-cdbc-1691-e063-6294a90ac6d2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204418
Listing Expiration 2026-12-31
Marketing Start 2015-08-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063791
Hyphenated Format 43063-791

Supplemental Identifiers

RxCUI
310410
UPC
0343063455906
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 ANDA204418 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-791-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-791-90)
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": "303d4c3e-cdbc-1691-e063-6294a90ac6d2", "openfda": {"upc": ["0343063455906"], "unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["726bb436-69e3-452f-9f28-153b58bf3ca5"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-791-30)", "package_ndc": "43063-791-30", "marketing_start_date": "20171002"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-791-90)", "package_ndc": "43063-791-90", "marketing_start_date": "20171018"}], "brand_name": "FOLIC ACID", "product_id": "43063-791_303d4c3e-cdbc-1691-e063-6294a90ac6d2", "dosage_form": "TABLET", "product_ndc": "43063-791", "generic_name": "folic acid", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FOLIC ACID", "active_ingredients": [{"name": "FOLIC ACID", "strength": "1 mg/1"}], "application_number": "ANDA204418", "marketing_category": "ANDA", "marketing_start_date": "20150804", "listing_expiration_date": "20261231"}