NDC 0093-7655 – Vardenafil Hydrochloride
Vardenafil Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-7655
Product details
- Brand name
- Vardenafil Hydrochloride
- Generic name
- Vardenafil Hydrochloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091347
- Marketed since
- January 3, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Vardenafil Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Vardenafil Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-7655-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7655-56) | Jan 3, 2019 |
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