Terbinafine Hydrochloride 55111-0250
Product NDC
55111-0250- Manufacturer
- Dr.reddys Laboratories Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 2, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA076390
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Terbinafine Hydrochloride | 250 mg/1 |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(5)
100 TABLET in 1 BOTTLE (55111-250-01)
500 TABLET in 1 BOTTLE (55111-250-05)
30 TABLET in 1 BOTTLE (55111-250-30)
10 BLISTER PACK in 1 CARTON (55111-250-79) / 10 TABLET in 1 BLISTER PACK (55111-250-78)
90 TABLET in 1 BOTTLE (55111-250-90)