NDC 71335-0918 – Terbinafine Hydrochloride
Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral
Product NDC71335-0918
Product details
- Brand name
- Terbinafine Hydrochloride
- Generic name
- Terbinafine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077714
- Marketed since
- December 27, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Allylamine Antifungal
Active ingredients
- Terbinafine Hydrochloride 250 mg/1
Uses, dosage, side effects and warnings for Terbinafine Hydrochloride →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0918-1 | 30 TABLET in 1 BOTTLE (71335-0918-1) | Jul 31, 2018 |
| 71335-0918-2 | 60 TABLET in 1 BOTTLE (71335-0918-2) | May 29, 2024 |
| 71335-0918-3 | 90 TABLET in 1 BOTTLE (71335-0918-3) | Jul 26, 2022 |
| 71335-0918-4 | 100 TABLET in 1 BOTTLE (71335-0918-4) | May 29, 2024 |
| 71335-0918-5 | 7 TABLET in 1 BOTTLE (71335-0918-5) | May 29, 2024 |
| 71335-0918-6 | 40 TABLET in 1 BOTTLE (71335-0918-6) | May 29, 2024 |
| 71335-0918-7 | 45 TABLET in 1 BOTTLE (71335-0918-7) | Aug 13, 2018 |
| 71335-0918-8 | 14 TABLET in 1 BOTTLE (71335-0918-8) | Sep 20, 2018 |
| 71335-0918-9 | 28 TABLET in 1 BOTTLE (71335-0918-9) | Dec 28, 2021 |
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