NDC 69097-859 – Terbinafine
Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral
Product NDC69097-859
Product details
- Brand name
- Terbinafine
- Generic name
- Terbinafine
- Labeler
- Cipla USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077533
- Marketed since
- June 27, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Allylamine Antifungal
Active ingredients
- Terbinafine Hydrochloride 250 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 69097-859-02 | 30 TABLET in 1 BOTTLE (69097-859-02) | Jun 27, 2016 |
| 69097-859-07 | 100 TABLET in 1 BOTTLE (69097-859-07) | Jun 27, 2016 |
| 69097-859-12 | 500 TABLET in 1 BOTTLE (69097-859-12) | Jun 27, 2016 |
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