NDC 71335-0881 – Amiodarone Hydrochloride
Amiodarone Hydrochloride 200 mg/1 · Tablet · Oral
Product NDC71335-0881
Product details
- Brand name
- Amiodarone Hydrochloride
- Generic name
- Amiodarone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075424
- Marketed since
- March 30, 2001
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antiarrhythmic
Active ingredients
- Amiodarone Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Amiodarone Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0881-1 | 200 TABLET in 1 BOTTLE (71335-0881-1) | Dec 27, 2021 |
| 71335-0881-2 | 30 TABLET in 1 BOTTLE (71335-0881-2) | Jan 3, 2019 |
| 71335-0881-3 | 60 TABLET in 1 BOTTLE (71335-0881-3) | Dec 27, 2021 |
| 71335-0881-4 | 90 TABLET in 1 BOTTLE (71335-0881-4) | Jun 26, 2018 |
| 71335-0881-5 | 10 TABLET in 1 BOTTLE (71335-0881-5) | Dec 27, 2021 |
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