Zolmitriptan
- Product NDC
- 68382-717
- 11-digit product format
- 683820717
- Labeler code
- 68382
- Product ID
- 68382-717_c8bbe1ff-34e4-4638-ac8a-00b1ceb2f310
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zolmitriptan
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA202890
- Marketing category
- ANDA
- Marketing start
- 2013-05-16
- Substance
- ZOLMITRIPTAN
- Active strength
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zolmitriptan
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZOLMITRIPTAN | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2FS66TH3YW |
| Rxcui | 284201, 351134 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68382-717-01 | Zolmitriptan | 100 in 1 BOTTLE | TABLET, ORALLY DISINTEGRATING | 100 | | 8 |
| 68382-717-06 | Zolmitriptan | 30 in 1 BOTTLE | TABLET, ORALLY DISINTEGRATING | 30 | | 8 |
| 68382-717-10 | Zolmitriptan | 1000 in 1 BOTTLE | TABLET, ORALLY DISINTEGRATING | 1000 | | 8 |
| 68382-717-16 | Zolmitriptan | 90 in 1 BOTTLE | TABLET, ORALLY DISINTEGRATING | 90 | | 8 |
| 68382-717-30 | Zolmitriptan | 10 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 10 | | 8 |
| 68382-717-77 | Zolmitriptan | 10 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 10 | | 8 |
| 68382-717-82 | Zolmitriptan | 1 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 1 | | 8 |
| 68382-717-87 | Zolmitriptan | 3 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 3 | | 8 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| ZOLMITRIPTAN | ACTIVE INGREDIENT | 2FS66TH3YW | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| ZOLMITRIPTAN | ACTIVE MOIETY | 2FS66TH3YW | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| ANHYDROUS CITRIC ACID | INACTIVE INGREDIENT | XF417D3PSL | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| ASPARTAME | INACTIVE INGREDIENT | Z0H242BBR1 | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| COLLOIDAL SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| CROSPOVIDONE | INACTIVE INGREDIENT | 68401960MK | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| GELATIN | INACTIVE INGREDIENT | 2G86QN327L | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| ORANGE | INACTIVE INGREDIENT | 5EVU04N5QU | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| POLACRILIN POTASSIUM | INACTIVE INGREDIENT | 0BZ5A00FQU | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
| SODIUM STEARYL FUMARATE | INACTIVE INGREDIENT | 7CV7WJK4UI | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS (USA) INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68382-717 | ZOLMITRIPTAN TABLET, ORALLY DISINTEGRATING [ZYDUS PHARMACEUTICALS USA INC.] | 8 | Current NDC, Legacy NDC, 8 package rows | 20231110_7fc95729-2f5d-4d5c-b26c-3a13854f73e3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-717-01 | 68382071701 | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-717-01) | | 2013-05-16 | 0000-00-00 | No | No | Current |
| 68382-717-06 | 68382071706 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-717-06) | | 2013-05-16 | 0000-00-00 | No | No | Current |
| 68382-717-10 | 68382071710 | 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-717-10) | | 2013-05-16 | 0000-00-00 | No | No | Current |
| 68382-717-16 | 68382071716 | 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-717-16) | | 2013-05-16 | 0000-00-00 | No | No | Current |
| 68382-717-30 | 68382071730 | 10 in 1 BLISTER PACK | | | | | | Historical |
| 68382-717-77 | 68382071777 | 10 BLISTER PACK in 1 CARTON (68382-717-77) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-717-30) | 10 blister pack | 2013-05-16 | 0000-00-00 | No | No | Current |
| 68382-717-82 | 68382071782 | 1 BLISTER PACK in 1 CARTON (68382-717-82) / 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-717-87) | 1 blister pack | 2013-05-16 | 0000-00-00 | No | No | Current |
| 68382-717-87 | 68382071787 | 3 in 1 BLISTER PACK | | | | | | Historical |