United States · FDA National Drug Code directory
Folixia
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 85477-902_4aa3e0fa-38cd-3f45-e063-6394a90a9a2b
- Product NDC
- 85477-902
- Form
- TABLET
- Composition / generic term
- Multivitamin
- Labeler
- Oncora Pharma, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20250224
- Source listing expiry
- 20271231
Source-listed ingredients
- FERROUS BISGLYCINATE — 20 mg/1
- POTASSIUM IODIDE — .15 mg/1
- PYRIDOXINE HYDROCHLORIDE — 26 mg/1
- BETA CAROTENE — .3 mg/1
- ASCORBIC ACID — 60 mg/1
- CHOLECALCIFEROL — .1 mg/1
- BIOTIN — .28 mg/1
- FOLIC ACID — 1.67 mg/1
- CYANOCOBALAMIN — .013 mg/1
- CALCIUM CARBONATE — 80 mg/1
- MAGNESIUM OXIDE — 25 mg/1
- .ALPHA.-TOCOPHEROL ACETATE, DL- — 4.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (85477-902-30) · 85477-902-30
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →