Prescription drug · ANDA
Folic Acid NDC 71335-0613
Folic acid 1 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-0613-1 | 71335061301 | 30 TABLET in 1 BOTTLE (71335-0613-1)Marketed from Jul 14, 2021 | |
| 71335-0613-2 | 71335061302 | 100 TABLET in 1 BOTTLE (71335-0613-2)Marketed from Jun 9, 2021 | |
| 71335-0613-3 | 71335061303 | 120 TABLET in 1 BOTTLE (71335-0613-3)Marketed from Jan 28, 2025 | |
| 71335-0613-4 | 71335061304 | 50 TABLET in 1 BOTTLE (71335-0613-4)Marketed from Jan 28, 2025 | |
| 71335-0613-5 | 71335061305 | 90 TABLET in 1 BOTTLE (71335-0613-5)Marketed from Jan 28, 2025 | |
| 71335-0613-6 | 71335061306 | 60 TABLET in 1 BOTTLE (71335-0613-6)Marketed from Jan 28, 2025 | |
| 71335-0613-7 | 71335061307 | 10 TABLET in 1 BOTTLE (71335-0613-7)Marketed from Jan 28, 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 204418
- Marketing start
- Listing expires
- Identifiers
- Product ID 71335-0613_9ef6c79d-7b8c-4f31-b0ba-543681121933SPL ID 9ef6c79d-7b8c-4f31-b0ba-543681121933SPL set ID 0e7cb7ea-c94e-4ce6-8149-311dc9c94e03RxCUI 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
N471335061301followed by a unit qualifier and the quantityPackage 71335-0613-01. 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 AND USAGE Folic acid, USP is effective in the treatment of megaloblastic anemias due to a deficiency of folic acid, USP (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 204418
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 | A-S Medication Solutions | 50090-3119 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | A-S Medication Solutions | 50090-6760 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 43063-791 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | DIRECT RX | 72189-199 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2557 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | SUNRISE PHARMACEUTICAL, INC. | 11534-165 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | Coupler LLC | 67046-0719 |
| Folic Acid | Folic acid 1 mg/1 | TabletOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-656 |