Diltiazem Hydrochloride
- Product NDC
- 68071-4371
- 11-digit product format
- 680714371
- Labeler code
- 68071
- Product ID
- 68071-4371_bb7bc6d4-7e36-01da-e053-2995a90a138e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075116
- Marketing category
- ANDA
- Marketing start
- 1999-12-28
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 120 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 |
|---|
| 68071-4371-9 | 68071437109 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-4371-9) | 2018-04-04 | 0000-00-00 | No | No | Current |