Diltiazem Hydrochloride
- Product NDC
- 70518-1096
- 11-digit product format
- 705181096
- Labeler code
- 70518
- Product ID
- 70518-1096_e2c29469-c1a4-8a61-e053-2995a90a74de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA018602
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-04-03
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 90 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1096-0 | 70518109600 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-1096-0) | 180 tablet | 2018-04-03 | 0000-00-00 | No | No | Current |