Diltiazem Hydrochloride
- Product NDC
- 70934-565
- 11-digit product format
- 709340565
- Labeler code
- 70934
- Product ID
- 70934-565_ac10ed43-3132-f1c3-e053-2a95a90a763c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA205231
- Marketing category
- ANDA
- Marketing start
- 2020-02-24
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 240 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70934-565-30 | 70934056530 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-565-30) | 2020-02-24 | 0000-00-00 | No | No | Current |