Diltiazem Hydrochloride
- Product NDC
- 63629-7232
- 11-digit product format
- 636297232
- Labeler code
- 63629
- Product ID
- 63629-7232_d1eb3111-662d-494b-95d3-29fd875abcfb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090492
- Marketing category
- ANDA
- Marketing start
- 2011-10-31
- 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
- 2021-12-31
- 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 |
|---|
| 63629-7232-1 | 63629723201 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-7232-1) | 2017-03-22 | 0000-00-00 | No | No | Current |
| 63629-7232-2 | 63629723202 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-7232-2) | 2017-03-22 | 0000-00-00 | No | No | Current |