Zolmitriptan
- Product NDC
- 73358-101
- 11-digit product format
- 733580101
- Labeler code
- 73358
- Product ID
- 73358-101_051aad90-fa90-45c5-ac00-4402be71778f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zolmitriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Curae Pharma360 Inc
- Application
- ANDA207867
- Marketing category
- ANDA
- Marketing start
- 2022-07-27
- Marketing end
- 0000-00-00
- Substance
- ZOLMITRIPTAN
- Active strength
- 3 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73358-101-06 | 73358010106 | 1 BLISTER PACK in 1 CARTON (73358-101-06) > 6 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2022-07-27 | 0000-00-00 | No | No | Current |