folic acid
Generic: folic acid
Labeler: direct rxDrug Facts
Product Profile
Brand Name
folic acid
Generic Name
folic acid
Labeler
direct rx
Dosage Form
TABLET
Routes
Active Ingredients
folic acid 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-199
Product ID
72189-199_2be95d4a-3002-97e4-e063-6294a90a5f3f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204418
Listing Expiration
2026-12-31
Marketing Start
2021-04-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189199
Hyphenated Format
72189-199
Supplemental Identifiers
RxCUI
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 (72189-199-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be95d4a-3002-97e4-e063-6294a90a5f3f", "openfda": {"unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["bfcb0849-6d9b-7705-e053-2a95a90a6541"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-199-30)", "package_ndc": "72189-199-30", "marketing_start_date": "20210412"}], "brand_name": "Folic Acid", "product_id": "72189-199_2be95d4a-3002-97e4-e063-6294a90a5f3f", "dosage_form": "TABLET", "product_ndc": "72189-199", "generic_name": "Folic Acid", "labeler_name": "DIRECT RX", "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": "20210412", "listing_expiration_date": "20261231"}