Prescription drug · ANDA
Topiramate NDC 71335-0325
Topiramate 100 mg/1 · Tablet, Film coated · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-0325-1 | 71335032501 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0325-1)Marketed from Nov 27, 2018 | |
| 71335-0325-2 | 71335032502 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0325-2)Marketed from Dec 28, 2018 | |
| 71335-0325-3 | 71335032503 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0325-3)Marketed from Nov 26, 2018 | |
| 71335-0325-4 | 71335032504 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0325-4)Marketed from Mar 9, 2022 | |
| 71335-0325-5 | 71335032505 | 50 TABLET, FILM COATED in 1 BOTTLE (71335-0325-5)Marketed from Mar 9, 2022 | |
| 71335-0325-6 | 71335032506 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0325-6)Marketed from May 23, 2019 | |
| 71335-0325-7 | 71335032507 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-0325-7)Marketed from Mar 9, 2022 | |
| 71335-0325-8 | 71335032508 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0325-8)Marketed from May 23, 2019 |
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)
- Topiramate
- Generic name (nonproprietary)
- topiramate
- Active ingredients
- Topiramate — 100 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090278
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2C19 Inhibitors (Mechanism)Cytochrome P450 3A4 Inducers (Mechanism)Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
- Identifiers
- Product ID 71335-0325_149ccab0-611c-4f69-b945-6201249eaac0SPL ID 149ccab0-611c-4f69-b945-6201249eaac0SPL set ID 484c132f-3d3d-4218-b22f-82e9b56cc2f4RxCUI 199889UNII 0H73WJJ391
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
N471335032501followed by a unit qualifier and the quantityPackage 71335-0325-01. 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)
Topiramate is indicated for: Epilepsy: initial monotherapy for the treatment of partial-onset or primary generalized tonic-clonic seizures in patients 2 years of age and older (1.1); adjunctive therapy for the treatment of partial-onset seizures, primary generalized tonic-clonic seizures, or seizures associated with Lennox- Gastaut syndrome in patients 2 years of age and older (1.2) Preventive treatment of migraine in patients 12 years of age and older (1.3) 1.1 Monotherapy Epilepsy Topiramate tablets are indicated as initial monotherapy for the treatment of partial-onset or primary generalized tonic-clonic seizures in patients 2 years of age and older. 1.2 Adjunctive Therapy Epilepsy Topira…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 090278
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 |
|---|---|---|---|---|
| Topiramate | Topiramate 100 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-004 |
| Topiramate | Topiramate 200 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-0925 |
| Topiramate | Topiramate 50 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-5165 |
| Topiramate | Topiramate 50 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-0487 |
| Topiramate | Topiramate 50 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 47335-710 |
| Topiramate | Topiramate 25 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 47335-707 |
| Topiramate | Topiramate 100 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 47335-711 |
| Topiramate | Topiramate 200 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 47335-712 |
| Topiramate | Topiramate 25 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-998 |
| Topiramate | Topiramate 25 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-0548 |
| Topiramate | Topiramate 50 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-997 |
| Topiramate | Topiramate 100 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 63187-801 |
| Topiramate | Topiramate 100 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 62756-711 |
| Topiramate | Topiramate 25 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 62756-707 |
| Topiramate | Topiramate 50 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 62756-710 |
| Topiramate | Topiramate 200 mg/1 | Tablet, Film coatedOral | Sun Pharmaceutical Industries, Inc. | 62756-712 |
| Topiramate | Topiramate 100 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 63187-060 |
| Topiramate | Topiramate 25 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-214 |
| Topiramate | Topiramate 50 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 63187-059 |
| Topiramate | Topiramate 25 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 63187-077 |
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