Diltiazem Hydrochloride
- Product NDC
- 70518-0109
- 11-digit product format
- 705180109
- Labeler code
- 70518
- Product ID
- 70518-0109_e6d99d37-e30a-52f0-e053-2995a90ae1ae
- 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
- 2017-01-09
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 30 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 |
|---|
| 70518-0109-0 | 70518010900 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0109-0) | | 2017-01-09 | 0000-00-00 | No | No | Current |
| 70518-0109-1 | 70518010901 | 100 POUCH in 1 BOX (70518-0109-1) > 1 TABLET, FILM COATED in 1 POUCH (70518-0109-2) | 100 pouch | 2022-08-22 | 0000-00-00 | No | No | Current |