Amiodarone hydrochloride
- Product NDC
- 65841-841
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amiodarone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA079029
- Marketing category
- ANDA
- Substance
- AMIODARONE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 65841-841-06 | 30 TABLET in 1 BOTTLE (65841-841-06) | 2023-02-09 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| AMIODARONE HYDROCHLORIDE TABLETS | Zydus Lifesciences Limited | 2024-11-25 | HUMAN PRESCRIPTION DRUG LABEL | 10 |