Diltiazem Hydrochloride
- Product NDC
- 0615-8129
- 11-digit product format
- 006158129
- Labeler code
- 0615
- Product ID
- 0615-8129_8c619aea-a944-46de-a20d-a6390882eabc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA075116
- Marketing category
- ANDA
- Marketing start
- 1999-12-28
- Marketing end
- 2022-06-30
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 240 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 |
|---|
| 0615-8129-39 | 00615812939 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8129-39) | 2019-01-09 | 2022-06-30 | No | No | Current |