folic acid
Generic: folic acid
Labeler: quagen pharmaceuticals llcDrug Facts
Product Profile
Brand Name
folic acid
Generic Name
folic acid
Labeler
quagen pharmaceuticals llc
Dosage Form
TABLET
Routes
Active Ingredients
folic acid 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70752-231
Product ID
70752-231_4a4f7bbb-97a0-4ac3-a044-1059d5e772ba
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091145
Listing Expiration
2026-12-31
Marketing Start
2023-07-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70752231
Hyphenated Format
70752-231
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA091145 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (70752-231-10)
- 1000 TABLET in 1 BOTTLE (70752-231-11)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a4f7bbb-97a0-4ac3-a044-1059d5e772ba", "openfda": {"unii": ["935E97BOY8"], "rxcui": ["310410"], "spl_set_id": ["354366ea-3702-4706-9fc0-0244b7278bd8"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70752-231-10)", "package_ndc": "70752-231-10", "marketing_start_date": "20230710"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70752-231-11)", "package_ndc": "70752-231-11", "marketing_start_date": "20230710"}], "brand_name": "Folic Acid", "product_id": "70752-231_4a4f7bbb-97a0-4ac3-a044-1059d5e772ba", "dosage_form": "TABLET", "product_ndc": "70752-231", "generic_name": "Folic Acid", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Folic Acid", "active_ingredients": [{"name": "FOLIC ACID", "strength": "1 mg/1"}], "application_number": "ANDA091145", "marketing_category": "ANDA", "marketing_start_date": "20230710", "listing_expiration_date": "20261231"}