Diltiazem Hydrochloride
- Product NDC
- 63629-3649
- 11-digit product format
- 636293649
- Labeler code
- 63629
- Product ID
- 63629-3649_001826f4-f531-454e-a37a-e4e0b147f61b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074185
- Marketing category
- ANDA
- Marketing start
- 1995-12-22
- Marketing end
- 0000-00-00
- Substance
- DILTIAZEM HYDROCHLORIDE
- Active strength
- 60 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 |
|---|
| 63629-3649-1 | 63629364901 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-3649-1) | 2007-10-26 | 0000-00-00 | No | No | Current |
| 63629-3649-2 | 63629364902 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-3649-2) | 2011-08-01 | 0000-00-00 | No | No | Current |
| 63629-3649-3 | 63629364903 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-3649-3) | 2012-05-08 | 0000-00-00 | No | No | Current |
| 63629-3649-4 | 63629364904 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-3649-4) | 2021-12-22 | 0000-00-00 | No | No | Current |