Diltiazem Hydrochloride
- Product NDC
- 42291-184
- 11-digit product format
- 422910184
- Labeler code
- 42291
- Product ID
- 42291-184_e0c99000-341c-7b44-e053-2995a90a2d58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- CAPSULE, COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA074984
- Marketing category
- ANDA
- Marketing start
- 2016-10-05
- Marketing end
- 2023-08-31
- 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
- 0000-00-00
- 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 |
|---|
| 42291-184-50 | 42291018450 | 500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (42291-184-50) | 2016-10-05 | 0000-00-00 | No | No | Current |
| 42291-184-90 | 42291018490 | 90 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (42291-184-90) | 2016-10-05 | 0000-00-00 | No | No | Current |