Zolmitriptan
- Product NDC
- 62332-462
- 11-digit product format
- 623320462
- Labeler code
- 62332
- Product ID
- 62332-462_e476239f-aad2-4fa7-8413-cfbe80600697
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolmitriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Alembic Pharmaceuticals Inc.
- Application
- ANDA204232
- Marketing category
- ANDA
- Marketing start
- 2024-01-10
- Substance
- ZOLMITRIPTAN
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2FS66TH3YW | ZOLMITRIPTAN | 139264-17-8 | ZOLMITRIPTAN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 62332-462-06 | 62332046206 | 6 TABLET, FILM COATED in 1 CARTON (62332-462-06) | 2024-01-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Zolmitriptan | Alembic Pharmaceuticals Inc. | Alembic Pharmaceuticals Limited | 2024-01-12 | Human Prescription Drug Label | 2 |