NDC 71335-9677 – Terbinafine hydrochloride
Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral
Product NDC71335-9677
Product details
- Brand name
- Terbinafine hydrochloride
- Generic name
- Terbinafine hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078163
- Marketed since
- January 28, 2022
- 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 |
|---|---|---|
| 71335-9677-1 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-9677-1) | Jun 6, 2023 |
| 71335-9677-2 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-9677-2) | Feb 3, 2025 |
| 71335-9677-3 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-9677-3) | Aug 30, 2023 |
| 71335-9677-4 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-9677-4) | Feb 3, 2025 |
| 71335-9677-5 | 7 TABLET in 1 BOTTLE, PLASTIC (71335-9677-5) | Feb 3, 2025 |
| 71335-9677-6 | 40 TABLET in 1 BOTTLE, PLASTIC (71335-9677-6) | Feb 3, 2025 |
| 71335-9677-7 | 45 TABLET in 1 BOTTLE, PLASTIC (71335-9677-7) | Jun 26, 2023 |
| 71335-9677-8 | 14 TABLET in 1 BOTTLE, PLASTIC (71335-9677-8) | May 10, 2023 |
| 71335-9677-9 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-9677-9) | May 10, 2023 |
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