Diltiazem Hydrochloride
- Product NDC
- 70518-3337
- 11-digit product format
- 705183337
- Labeler code
- 70518
- Product ID
- 70518-3337_d80f12c8-0d5e-322a-e053-2995a90a56d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205231
- Marketing category
- ANDA
- Marketing start
- 2022-01-20
- 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
- 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 |
|---|
| 70518-3337-0 | 70518333700 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3337-0) | 2022-01-20 | 0000-00-00 | No | No | Current |