folic acid
Generic: folic acid
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
folic acid
Generic Name
folic acid
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
folic acid 1 mg/1
Manufacturer
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
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-791-30)
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-791-90)
Packages (2)
Ingredients (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"}