NDC 68462-260 – Verapamil hydrochloride
Verapamil Hydrochloride 240 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68462-260
Product details
- Brand name
- Verapamil hydrochloride
- Generic name
- Verapamil hydrochloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078906
- Marketed since
- September 17, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Calcium Channel Blocker
Active ingredients
- Verapamil Hydrochloride 240 mg/1
Uses, dosage, side effects and warnings for Verapamil Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68462-260-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-260-01) | Sep 17, 2009 |
| 68462-260-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-260-05) | Sep 17, 2009 |
| 68462-260-10 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-260-10) | Sep 17, 2009 |
| 68462-260-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-260-30) | Sep 17, 2009 |
| 68462-260-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-260-90) | Sep 17, 2009 |
Recalls mentioning this NDC
- D-0483-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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