Eletriptan Hydrobromide
- Product NDC
- 65162-042
- 11-digit product format
- 651620042
- Labeler code
- 65162
- Product ID
- 65162-042_52ee20ae-6bf7-4834-a483-3e010b0106d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eletriptan Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals LLC
- Application
- ANDA206787
- Marketing category
- ANDA
- Marketing start
- 2018-05-30
- Marketing end
- 0000-00-00
- Substance
- ELETRIPTAN HYDROBROMIDE MONOHYDRATE
- 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
- 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 |
|---|
| 65162-042-03 | 65162004203 | 30 TABLET, FILM COATED in 1 BOTTLE (65162-042-03) | | 2018-06-02 | 0000-00-00 | No | No | Current |
| 65162-042-80 | 65162004280 | 1 BLISTER PACK in 1 CARTON (65162-042-80) > 6 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2018-05-30 | 0000-00-00 | No | No | Current |