DILTIAZEM HYDROCHLORIDE
- Product NDC
- 70934-210
- 11-digit product format
- 709340210
- Labeler code
- 70934
- Product ID
- 70934-210_b8b5ff57-8370-1194-e053-2995a90ae8f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DILTIAZEM HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA074943
- Marketing category
- ANDA
- Marketing start
- 2018-12-18
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 180 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-210-30 | 70934021030 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-210-30) | 2018-12-18 | 0000-00-00 | No | No | Current |