Eletriptan
- Product NDC
- 59762-2321
- 11-digit product format
- 597622321
- Labeler code
- 59762
- Product ID
- 59762-2321_e1db233f-7b92-4130-9dfa-8927a81d2f51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eletriptan hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA021016
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-07-24
- Marketing end
- 0000-00-00
- Substance
- ELETRIPTAN HYDROBROMIDE
- Active strength
- 20 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
- 2022-12-31
- 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 |
|---|
| 59762-2321-1 | 59762232101 | 6 BLISTER PACK in 1 CARTON (59762-2321-1) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2017-07-24 | 0000-00-00 | No | No | Current |