Diltiazem Hydrochloride
- Product NDC
- 70518-2506
- 11-digit product format
- 705182506
- Labeler code
- 70518
- Product ID
- 70518-2506_dc113c6c-0815-455d-e053-2995a90a4c8e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205231
- Marketing category
- ANDA
- Marketing start
- 2019-12-24
- 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
- 2023-12-31
- 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 |
|---|
| 70518-2506-0 | 70518250600 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2506-0) | 2019-12-24 | 0000-00-00 | No | No | Current |