diltiazem hydrochloride
- Product NDC
- 68788-7634
- 11-digit product format
- 687887634
- Labeler code
- 68788
- Product ID
- 68788-7634_fe289d4b-c361-479a-a024-fce9b73b724b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diltiazem hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA206534
- Marketing category
- ANDA
- Marketing start
- 2020-03-06
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 120 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7634-1 | 68788763401 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-7634-1) | 2020-03-06 | 0000-00-00 | No | No | Current |
| 68788-7634-3 | 68788763403 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-7634-3) | 2020-03-06 | 0000-00-00 | No | No | Current |
| 68788-7634-6 | 68788763406 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-7634-6) | 2020-03-06 | 0000-00-00 | No | No | Current |
| 68788-7634-8 | 68788763408 | 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-7634-8) | 2020-03-06 | 0000-00-00 | No | No | Current |
| 68788-7634-9 | 68788763409 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-7634-9) | 2020-03-06 | 0000-00-00 | No | No | Current |