Prescription drug · ANDA
Folic Acid NDC 71335-2547
Folic acid 1 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-2547-1 | 71335254701 | 30 TABLET in 1 BOTTLE (71335-2547-1)Marketed from Jan 21, 2025 | |
| 71335-2547-2 | 71335254702 | 100 TABLET in 1 BOTTLE (71335-2547-2)Marketed from Jan 21, 2025 | |
| 71335-2547-3 | 71335254703 | 120 TABLET in 1 BOTTLE (71335-2547-3)Marketed from Jan 21, 2025 | |
| 71335-2547-4 | 71335254704 | 50 TABLET in 1 BOTTLE (71335-2547-4)Marketed from Jan 21, 2025 | |
| 71335-2547-5 | 71335254705 | 90 TABLET in 1 BOTTLE (71335-2547-5)Marketed from Jan 21, 2025 | |
| 71335-2547-6 | 71335254706 | 60 TABLET in 1 BOTTLE (71335-2547-6)Marketed from Jan 21, 2025 | |
| 71335-2547-7 | 71335254707 | 10 TABLET in 1 BOTTLE (71335-2547-7)Marketed from Jan 21, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Folic Acid
- Generic name (nonproprietary)
- folic acid
- Active ingredients
- Folic acid — 1 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 202437
- Marketing start
- Listing expires
- Identifiers
- Product ID 71335-2547_b55fa556-0793-465c-9d62-2f21ff5331b5SPL ID b55fa556-0793-465c-9d62-2f21ff5331b5SPL set ID ceedca87-e390-4123-8de5-8c2a28bd0377RxCUI 310410UNII 935E97BOY8
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471335254701followed by a unit qualifier and the quantityPackage 71335-2547-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS & USAGE Folic acid, USP is effective in the treatment of megaloblastic anemias due to a deficiency of folic acid (as may be seen in tropical or nontropical sprue) and in anemias of nutritional origin, pregnancy, infancy, or childhood.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 202437
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Folic Acid | Folic acid 1 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2413 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8827 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | Coupler LLC | 67046-1449 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | Cadila Pharmaceuticals Limited | 71209-007 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4338 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | Modavar Pharmaceuticals LLC | 72241-050 |