Diltiazem Hydrochloride
- Product NDC
- 42799-132
- 11-digit product format
- 427990132
- Labeler code
- 42799
- Product ID
- 42799-132_5b90e43a-b550-4a28-b9f8-5f1b4663201a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Edenbridge Pharmaceuticals LLC.
- Application
- ANDA211596
- Marketing category
- ANDA
- Marketing start
- 2018-10-29
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42799-132 | DILTIAZEM HYDROCHLORIDE TABLET, FILM COATED [EDENBRIDGE PHARMACEUTICALS LLC.] | 6 | Legacy NDC | 20220115_14a67570-6820-46ee-920c-b6d3663609d9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42799-132-01 | 42799013201 | 100 TABLET, FILM COATED in 1 BOTTLE (42799-132-01) | 2018-10-29 | 0000-00-00 | No | No | Current |