NDC 53746-669 – Acebutolol Hydrochloride
Acebutolol Hydrochloride 200 mg/1 · Capsule · Oral
Product NDC53746-669
Product details
- Brand name
- Acebutolol Hydrochloride
- Generic name
- Acebutolol Hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA075047
- Marketed since
- December 1, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Acebutolol Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Acebutolol Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 53746-669-01 | 100 CAPSULE in 1 BOTTLE (53746-669-01) | Dec 1, 2009 |
| 53746-669-05 | 500 CAPSULE in 1 BOTTLE (53746-669-05) | Dec 1, 2009 |
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