NDC 46708-238 – Vardenafil Hydrochloride
Vardenafil Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC46708-238
Product details
- Brand name
- Vardenafil Hydrochloride
- Generic name
- Vardenafil Hydrochloride
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA214031
- Marketed since
- August 5, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phosphodiesterase 5 Inhibitor
Active ingredients
- Vardenafil Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Vardenafil Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 46708-238-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-238-30) | Aug 5, 2020 |
| 46708-238-31 | 100 TABLET, FILM COATED in 1 BOTTLE (46708-238-31) | Aug 5, 2020 |
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