Diltiazem Hydrochloride
- Product NDC
- 70934-559
- 11-digit product format
- 709340559
- Labeler code
- 70934
- Product ID
- 70934-559_d4648d47-e444-6761-e053-2a95a90a1848
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- NDA018602
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-03-03
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-559-30 | 70934055930 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-559-30) | 30 tablet | 2020-03-03 | 0000-00-00 | No | No | Current |