NDC 68382-227 – Amiodarone hydrochloride

Amiodarone Hydrochloride 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-227

Product details

Brand name
Amiodarone hydrochloride
Generic name
Amiodarone hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA079029
Marketed since
August 10, 2009
Listing expires
December 31, 2026
Pharmacologic class
Antiarrhythmic

Active ingredients

Uses, dosage, side effects and warnings for Amiodarone Hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
68382-227-05500 TABLET in 1 BOTTLE (68382-227-05)Aug 10, 2009
68382-227-0630 TABLET in 1 BOTTLE (68382-227-06)Aug 10, 2009
68382-227-101000 TABLET in 1 BOTTLE (68382-227-10)Aug 10, 2009
68382-227-1460 TABLET in 1 BOTTLE (68382-227-14)Aug 10, 2009
68382-227-77100 BLISTER PACK in 1 CARTON (68382-227-77) / 1 TABLET in 1 BLISTER PACK (68382-227-30)Aug 10, 2009

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