Home NDC 85477-503 METAVEX
Product NDC 85477-503
11-digit product format 854770503
Labeler code 85477
Product ID 85477-503_0733c82d-8d75-4f70-9744-71e526509b95
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name METAVEX
Dosage form TABLET
Route ORAL
Labeler Oncora Pharma, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-01-01
Substance CHOLECALCIFEROL; FOLIC ACID; BLUE AGAVE INULIN (AGAVE TEQUILANA); ELM; ALOE FEROX LEAF; RHAMNUS CATHARTICA BARK
Active strength .125; 1; 500; 425; 225; 135 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
Pharmacologic classes Vitamin D [CS], Vitamin D [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base METAVEX
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHOLECALCIFEROL .125 mg/1 FOLIC ACID 1 mg/1 BLUE AGAVE INULIN (AGAVE TEQUILANA) 500 mg/1 ELM 425 mg/1 ALOE FEROX LEAF 225 mg/1 RHAMNUS CATHARTICA BARK 135 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
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 85477-503-30 METAVEX 1 in 1 BOTTLE TABLET 1 2
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 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85477-503-30 85477050330 1 TABLET in 1 BOTTLE (85477-503-30) 1 tablet 2026-01-01 No No Current