NDC 68462-292 – Verapamil hydrochloride
Verapamil Hydrochloride 120 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68462-292
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 · ANDA090700
- Marketed since
- August 5, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Calcium Channel Blocker
Active ingredients
- Verapamil Hydrochloride 120 mg/1
Uses, dosage, side effects and warnings for Verapamil Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-292-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-292-01) | Aug 5, 2011 |
| 68462-292-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-292-05) | Aug 5, 2011 |
| 68462-292-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-292-90) | Aug 5, 2011 |
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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