NDC 69097-996 – Diltiazem Hydrochloride
Diltiazem Hydrochloride 360 mg/1 · Tablet, Extended Release · Oral
Product NDC69097-996
Product details
- Brand name
- Diltiazem Hydrochloride
- Generic name
- Diltiazem hydrochloride
- Labeler
- Cipla USA, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216327
- Marketed since
- June 12, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Calcium Channel Blocker
Active ingredients
- Diltiazem Hydrochloride 360 mg/1
Uses, dosage, side effects and warnings for Diltiazem Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 69097-996-02 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-996-02) | Jun 12, 2023 |
| 69097-996-05 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-996-05) | Jun 12, 2023 |
Other Diltiazem Hydrochloride products
- 69097-997 Diltiazem Hydrochloride 420 mg/1 · Tablet, Extended Release · Cipla USA, Inc.
- 69097-992 Diltiazem Hydrochloride 120 mg/1 · Tablet, Extended Release · Cipla USA, Inc.
- 69097-995 Diltiazem Hydrochloride 300 mg/1 · Tablet, Extended Release · Cipla USA, Inc.
- 69097-993 Diltiazem Hydrochloride 180 mg/1 · Tablet, Extended Release · Cipla USA, Inc.
- 69097-994 Diltiazem Hydrochloride 240 mg/1 · Tablet, Extended Release · Cipla USA, Inc.
- 68682-705 Diltiazem Hydrochloride 180 mg/1 · Tablet, Extended Release · Oceanside Pharmaceuticals
- 68682-704 Diltiazem Hydrochloride 120 mg/1 · Tablet, Extended Release · Oceanside Pharmaceuticals
- 68682-708 Diltiazem Hydrochloride 360 mg/1 · Tablet, Extended Release · Oceanside Pharmaceuticals
- 68682-709 Diltiazem Hydrochloride 420 mg/1 · Tablet, Extended Release · Oceanside Pharmaceuticals
- 68682-706 Diltiazem Hydrochloride 240 mg/1 · Tablet, Extended Release · Oceanside Pharmaceuticals
- 68682-707 Diltiazem Hydrochloride 300 mg/1 · Tablet, Extended Release · Oceanside Pharmaceuticals
- 50228-498 Diltiazem Hydrochloride 300 mg/1 · Tablet, Extended Release · ScieGen Pharmaceuticals, Inc.