Home NDC 73308-501 FOLIC ACID
Product NDC 73308-501
11-digit product format 733080501
Labeler code 73308
Product ID 73308-501_f6a753c1-e141-42a5-b758-7faad81c9427
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name folic acid
Dosage form SOLUTION
Route ORAL
Labeler Ayurax, LLC
Application NDA216395
Marketing category NDA AUTHORIZED GENERIC
Marketing start 2026-01-28
Substance FOLIC ACID
Active strength 1 mg/5mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N216395-001 QUIOFIC FOLIC ACID 0.2MG/ML SOLUTION / ORAL RLD, RS 2026-01-26
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-02-19 14:30 UTC 2026-02 N216395-001 QUIOFIC 0.2MG/ML SOLUTION / ORAL RLD, RS 2026-01-26 011fe1cb6892…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N216395-001 QUIOFIC 0.2MG/ML SOLUTION / ORAL RLD, RS 2026-01-26 a50c72e98297…
Additional Listing Data#
Finished product Yes
Brand name base FOLIC ACID
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FOLIC ACID 1 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 935E97BOY8 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2707361 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73308-501-75 FOLIC ACID 75 mL in 1 BOTTLE SOLUTION 75 3
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 2 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73308-501-75 73308050175 75 mL in 1 BOTTLE (73308-501-75) 75 ml 2026-01-28 No No Current