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NDC 65162-0042-80 Eletriptan Hydrobromide 20 mg/1 Details
Eletriptan Hydrobromide 20 mg/1
Eletriptan Hydrobromide is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is ELETRIPTAN HYDROBROMIDE MONOHYDRATE.
MedlinePlus Drug Summary
Eletriptan is used to treat the symptoms of migraine headaches (severe throbbing headaches that sometimes are accompanied by nausea and sensitivity to sound and light). Eletriptan is in a class of medications called selective serotonin receptor agonists. It works by narrowing blood vessels in the brain, stopping pain signals from being sent to the brain, and blocking the release of certain natural substances that cause pain, nausea, and other symptoms of migraine. Eletriptan does not prevent migraine attacks or reduce the number of headaches you have.
Related Packages: 65162-0042-80Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Eletriptan
Product Information
| NDC | 65162-0042 |
|---|---|
| Product ID | 65162-042_a52e5add-18c4-4319-8fbc-3ad504d61057 |
| Associated GPIs | 67406025100320 |
| GCN Sequence Number | 049605 |
| GCN Sequence Number Description | eletriptan hydrobromide TABLET 20 MG ORAL |
| HIC3 | H3F |
| HIC3 Description | ANTIMIGRAINE PREPARATIONS |
| GCN | 15173 |
| HICL Sequence Number | 023093 |
| HICL Sequence Number Description | ELETRIPTAN HYDROBROMIDE |
| Brand/Generic | Generic |
| Proprietary Name | Eletriptan Hydrobromide |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Eletriptan Hydrobromide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | ELETRIPTAN HYDROBROMIDE MONOHYDRATE |
| Labeler Name | Amneal Pharmaceuticals LLC |
| Pharmaceutical Class | Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA206787 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65162-0042-80 (65162004280)
| NDC Package Code | 65162-042-80 |
|---|---|
| Billing NDC | 65162004280 |
| Package | 1 BLISTER PACK in 1 CARTON (65162-042-80) / 6 TABLET, FILM COATED in 1 BLISTER PACK |
| Marketing Start Date | 2018-05-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |