Prescription drug · ANDA
Rizatriptan NDC 71335-1352
Rizatriptan benzoate 10 mg/1 · Tablet, Film coated · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-1352-1 | 7133513520171335135201 | 10 TABLET, FILM COATED in 1 BLISTER PACK (71335-1352-1)Marketed from Sep 19, 2022 | |
| 71335-1352-2 | 7133513520271335135202 | 6 TABLET, FILM COATED in 1 BLISTER PACK (71335-1352-2)Marketed from Mar 8, 2021 | |
| 71335-1352-3 | 7133513520371335135203 | 90 TABLET, FILM COATED in 1 BLISTER PACK (71335-1352-3)Marketed from Sep 19, 2022 | |
| 71335-1352-4 | 7133513520471335135204 | 9 TABLET, FILM COATED in 1 BLISTER PACK (71335-1352-4)Marketed from Oct 1, 2019 | |
| 71335-1352-5 | 7133513520571335135205 | 30 TABLET, FILM COATED in 1 BLISTER PACK (71335-1352-5)Marketed from Sep 3, 2021 | |
| 71335-1352-6 | 7133513520671335135206 | 18 TABLET, FILM COATED in 1 BLISTER PACK (71335-1352-6)Marketed from Oct 11, 2019 | |
| 71335-1352-7 | 7133513520771335135207 | 12 TABLET, FILM COATED in 1 BLISTER PACK (71335-1352-7)Marketed from Jan 9, 2020 |
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)
- Rizatriptan
- Generic name (nonproprietary)
- rizatriptan
- Active ingredients
- Rizatriptan benzoate — 10 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 203147
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
- Identifiers
- Product ID 71335-1352_9f140953-589f-43ab-b977-a5c48c5853c1SPL ID 9f140953-589f-43ab-b977-a5c48c5853c1SPL set ID 7db81532-6781-47f7-a5cd-6aeda9b8bf6fRxCUI 314209UNII WR978S7QHH
- Pharmacologic class
- Serotonin-1b and Serotonin-1d Receptor Agonist
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
N471335135201followed by a unit qualifier and the quantityPackage 71335-1352-01. 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)
Ri zatriptan benzoate tablets are indicated for the acute treatment of migraine with or without aura in adults and in pediatric patients 6 to 17 years old. Limitations of Use • Rizatriptan benzoate tablets should only be used where a clear diagnosis of migraine has been established. If a patient has no response for the first migraine attack treated with rizatriptan benzoate tablets, the diagnosis of migraine should be reconsidered before rizatriptan benzoate tablets are administered to treat any subsequent attacks. • Rizatriptan benzoate tablets are not indicated for use in the management of hemiplegic or basilar migraine [see Contraindications (4) ]. • Rizatriptan benzoate tablets are not i…
Excerpt only. Read the full label for complete information.
About NDC 71335-1352
- What is NDC 71335-1352?
- 71335-1352 is the product NDC for Rizatriptan, Rizatriptan benzoate 10 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Rizatriptan.
- What is the active ingredient?
- Rizatriptan benzoate.
- Who is the labeler?
- Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Rizatriptan?
- 4 other product NDCs are listed under this name. See all Rizatriptan NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Rizatriptan products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Rizatriptan | Rizatriptan benzoate 5 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-087 | 33342-0087-0733342-0087-1233342-0087-41+4 more |
| Rizatriptan | Rizatriptan benzoate 10 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-088 | 33342-0088-0733342-0088-1233342-0088-41+4 more |
| Rizatriptan | Rizatriptan benzoate 10 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-7747 | 50090-7747-00 |
| Rizatriptan | Rizatriptan benzoate 10 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-2980 | 71335-2980-01 |
Other NDCs under ANDA 203147
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 |
|---|---|---|---|---|
| Rizatriptan | Rizatriptan benzoate 5 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-087 |
| Rizatriptan | Rizatriptan benzoate 10 mg/1 | Tablet, Film coatedOral | Macleods Pharmaceuticals Limited | 33342-088 |
| Rizatriptan | Rizatriptan benzoate 10 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-7747 |
| Rizatriptan | Rizatriptan benzoate 10 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-2980 |
| Rizatriptan Benzoate | Rizatriptan benzoate 10 mg/1 | Tablet, Film coatedOral | Direct_Rx | 72189-447 |