NDC 55111-250 – Terbinafine Hydrochloride
Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral
Product NDC55111-250
Product details
- Brand name
- Terbinafine Hydrochloride
- Generic name
- Terbinafine Hydrochloride
- Labeler
- Dr.Reddys Laboratories Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076390
- Marketed since
- July 2, 2007
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 55111-250-01 | 100 TABLET in 1 BOTTLE (55111-250-01) | Jul 2, 2007 |
| 55111-250-05 | 500 TABLET in 1 BOTTLE (55111-250-05) | Jul 2, 2007 |
| 55111-250-30 | 30 TABLET in 1 BOTTLE (55111-250-30) | Jul 2, 2007 |
| 55111-250-79 | 10 BLISTER PACK in 1 CARTON (55111-250-79) / 10 TABLET in 1 BLISTER PACK (55111-250-78) | Jul 2, 2007 |
| 55111-250-90 | 90 TABLET in 1 BOTTLE (55111-250-90) | Jul 2, 2007 |
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