NDC 68382-922 – Eletriptan hydrobromide
Eletriptan Hydrobromide 20 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-922
Product details
- Brand name
- Eletriptan hydrobromide
- Generic name
- Eletriptan hydrobromide
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206409
- Marketed since
- July 12, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin-1b and Serotonin-1d Receptor Agonist
Active ingredients
- Eletriptan Hydrobromide 20 mg/1
Uses, dosage, side effects and warnings for Eletriptan hydrobromide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68382-922-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-922-06) | Jul 12, 2017 |
| 68382-922-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-922-10) | Jul 12, 2017 |
| 68382-922-77 | 10 BLISTER PACK in 1 CARTON (68382-922-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-922-30) | Jul 12, 2017 |
| 68382-922-86 | 1 BLISTER PACK in 1 CARTON (68382-922-86) / 6 TABLET, FILM COATED in 1 BLISTER PACK | Jul 12, 2017 |
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