Diltiazem Hydrochloride
- Product NDC
- 70518-2683
- 11-digit product format
- 705182683
- Labeler code
- 70518
- Product ID
- 70518-2683_c7177cc3-2688-c727-e053-2995a90afe1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074185
- Marketing category
- ANDA
- Marketing start
- 2020-04-08
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2683-0 | 70518268300 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2683-0) | | 2020-04-08 | 0000-00-00 | No | No | Current |
| 70518-2683-1 | 70518268301 | 100 POUCH in 1 BOX (70518-2683-1) > 1 TABLET, FILM COATED in 1 POUCH (70518-2683-2) | 100 pouch | 2021-07-13 | 0000-00-00 | No | No | Current |