NDC 70518-1326 – Verapamil hydrochloride
Verapamil Hydrochloride 240 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70518-1326
Product details
- Brand name
- Verapamil hydrochloride
- Generic name
- Verapamil hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078906
- Marketed since
- July 26, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Calcium Channel Blocker
Active ingredients
- Verapamil Hydrochloride 240 mg/1
Uses, dosage, side effects and warnings for Verapamil Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70518-1326-0 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1326-0) | Jul 30, 2018 |
| 70518-1326-1 | 50 POUCH in 1 BOX (70518-1326-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1326-2) | Apr 27, 2026 |
| 70518-1326-3 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1326-3) | May 13, 2026 |
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