Diltiazem Hydrochloride
- Product NDC
- 50090-7401
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diltiazem Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA216521
- Marketing category
- ANDA
- Substance
- DILTIAZEM HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-7401-2 | 30 TABLET in 1 BOTTLE (50090-7401-2) | 2024-10-24 | No | Historical | |
| 50090-7401-3 | 90 TABLET in 1 BOTTLE (50090-7401-3) | 2024-10-24 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Diltiazem Hydrochloride Tablets, USP Tablets | A-S Medication Solutions | 2024-10-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |