Naratriptan
- Product NDC
- 50090-6162
- 11-digit product format
- 500906162
- Labeler code
- 50090
- Product ID
- 50090-6162_4f5b1665-0046-4dad-9d14-e2fe9c8b1c81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naratriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091441
- Marketing category
- ANDA
- Marketing start
- 2022-04-11
- Marketing end
- 0000-00-00
- Substance
- NARATRIPTAN HYDROCHLORIDE
- 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 |
|---|
| 50090-6162-0 | 50090616200 | 1 BLISTER PACK in 1 CARTON (50090-6162-0) > 9 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2022-10-11 | 0000-00-00 | No | No | Current |