folic acid

Generic: folic acid

Labeler: ayurax, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name folic acid
Generic Name folic acid
Labeler ayurax, llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

folic acid 1 mg/5mL

Manufacturer
Ayurax, LLC

Identifiers & Regulatory

Product NDC 73308-501
Product ID 73308-501_f6a753c1-e141-42a5-b758-7faad81c9427
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA216395
Listing Expiration 2027-12-31
Marketing Start 2026-01-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73308501
Hyphenated Format 73308-501

Supplemental Identifiers

RxCUI
2707361
UPC
0373308501754
UNII
935E97BOY8

Packaging Origin

Original Packager
true

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 NDA216395 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/5mL
source: ndc
Packaging
  • 75 mL in 1 BOTTLE (73308-501-75)
source: ndc

Packages (1)

73308-501-75 75 mL in 1 BOTTLE (73308-501-75)

Ingredients (1)

folic acid (1 mg/5mL)

Linked Drug Pages (1)

FOLIC ACID ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f6a753c1-e141-42a5-b758-7faad81c9427", "openfda": {"upc": ["0373308501754"], "unii": ["935E97BOY8"], "rxcui": ["2707361"], "spl_set_id": ["96618bf8-6c03-4df3-9896-b7ef27ca392a"], "manufacturer_name": ["Ayurax, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (73308-501-75)", "package_ndc": "73308-501-75", "marketing_start_date": "20260128"}], "brand_name": "FOLIC ACID", "product_id": "73308-501_f6a753c1-e141-42a5-b758-7faad81c9427", "dosage_form": "SOLUTION", "product_ndc": "73308-501", "generic_name": "folic acid", "labeler_name": "Ayurax, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FOLIC ACID", "active_ingredients": [{"name": "FOLIC ACID", "strength": "1 mg/5mL"}], "application_number": "NDA216395", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20260128", "listing_expiration_date": "20271231"}