Sumatriptan
- Product NDC
- 16714-531
- 11-digit product format
- 167140531
- Labeler code
- 16714
- Product ID
- 16714-531_c432e027-e5f4-4d03-a4b8-a82a8f36857c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sumatriptan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA078284
- Marketing category
- ANDA
- Marketing start
- 2011-01-03
- Marketing end
- 2021-10-31
- Substance
- SUMATRIPTAN SUCCINATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC],Serotonin 1b Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 16714-531-11 | 16714053111 | 1 BLISTER PACK in 1 CARTON (16714-531-11) > 9 TABLET, FILM COATED in 1 BLISTER PACK (16714-531-10) | 1 blister pack | 2011-01-03 | 2021-10-31 | No | No | Current |