diltiazem hydrochloride
- Product NDC
- 50090-6155
- 11-digit product format
- 500906155
- Labeler code
- 50090
- Product ID
- 50090-6155_1bf3c802-9b25-4d1b-b58f-5219e36e7c80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diltiazem hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA206534
- Marketing category
- ANDA
- Marketing start
- 2017-09-28
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| OLH94387TE | DILTIAZEM HYDROCHLORIDE | 33286-22-5 | DILTIAZEM HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-6155-0 | 50090615500 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6155-0) | 2022-10-06 | 0000-00-00 | No | No | Current |
| 50090-6155-1 | 50090615501 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6155-1) | 2022-10-06 | 0000-00-00 | No | No | Current |