eletriptan hydrobromide
- Product NDC
- 71335-1830
- 11-digit product format
- 713351830
- Labeler code
- 71335
- Product ID
- 71335-1830_726323d8-c9a7-44c1-bb95-08b6c378332c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- eletriptan hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205186
- Marketing category
- ANDA
- Marketing start
- 2017-08-29
- Marketing end
- 0000-00-00
- Substance
- ELETRIPTAN HYDROBROMIDE
- Active strength
- 40 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1830-1 | 71335183001 | 9 TABLET, FILM COATED in 1 BLISTER PACK (71335-1830-1) | 2021-04-29 | 0000-00-00 | No | No | Current |
| 71335-1830-2 | 71335183002 | 30 TABLET, FILM COATED in 1 BLISTER PACK (71335-1830-2) | 2021-04-29 | 0000-00-00 | No | No | Current |