Diltiazem Hydrochloride
- Product NDC
- 68788-6893
- 11-digit product format
- 687886893
- Labeler code
- 68788
- Product ID
- 68788-6893_a58ab104-3d60-445c-9310-bdffd0d75f28
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090492
- Marketing category
- ANDA
- Marketing start
- 2017-02-10
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 180 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68788-6893-1 | 68788689301 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6893-1) | 2017-02-10 | 0000-00-00 | No | No | Current |
| 68788-6893-3 | 68788689303 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6893-3) | 2017-02-10 | 0000-00-00 | No | No | Current |
| 68788-6893-6 | 68788689306 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6893-6) | 2017-02-10 | 0000-00-00 | No | No | Current |
| 68788-6893-8 | 68788689308 | 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6893-8) | 2017-02-10 | 0000-00-00 | No | No | Current |
| 68788-6893-9 | 68788689309 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6893-9) | 2017-02-10 | 0000-00-00 | No | No | Current |