NDC 69452-351 – Terbinafine hydrochloride
Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral
Product NDC69452-351
Product details
- Brand name
- Terbinafine hydrochloride
- Generic name
- Terbinafine hydrochloride
- Labeler
- Bionpharma Inc.
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 69452-351-13 | 30 TABLET in 1 BOTTLE, PLASTIC (69452-351-13) | Jan 28, 2022 |
| 69452-351-20 | 100 TABLET in 1 BOTTLE, PLASTIC (69452-351-20) | Jan 28, 2022 |
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