Diltiazem Hydrochloride
- Product NDC
- 70518-0820
- 11-digit product format
- 705180820
- Labeler code
- 70518
- Product ID
- 70518-0820_e26e9400-7b7f-39b2-e053-2995a90a51a0
- 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
- 2017-11-06
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 60 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 |
|---|
| 70518-0820-0 | 70518082000 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0820-0) | 2017-11-06 | 0000-00-00 | No | No | Current |