NDC 0187-2048 – Cardizem LA
Diltiazem Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC0187-2048
Product details
- Brand name
- Cardizem LA
- Generic name
- Diltiazem Hydrochloride
- Labeler
- Bausch Health US LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- NDA · NDA021392
- Marketed since
- December 25, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Calcium Channel Blocker
Active ingredients
- Diltiazem Hydrochloride 300 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0187-2048-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2048-30) | Dec 25, 2010 |
| 0187-2048-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-2048-90) | Dec 25, 2010 |
Other Cardizem LA products
- 0187-2045 Diltiazem Hydrochloride 120 mg/1 · Tablet, Extended Release · Bausch Health US LLC
- 0187-2046 Diltiazem Hydrochloride 180 mg/1 · Tablet, Extended Release · Bausch Health US LLC
- 0187-2047 Diltiazem Hydrochloride 240 mg/1 · Tablet, Extended Release · Bausch Health US LLC
- 0187-2049 Diltiazem Hydrochloride 360 mg/1 · Tablet, Extended Release · Bausch Health US LLC
- 0187-2050 Diltiazem Hydrochloride 420 mg/1 · Tablet, Extended Release · Bausch Health US LLC