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NDC 51662-1205-03 AMIODARONE HYDROCHLORIDE 50 mg/mL Details
AMIODARONE HYDROCHLORIDE 50 mg/mL
AMIODARONE HYDROCHLORIDE is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by HF Acquisition Co LLC, DBA HealthFirst. The primary component is AMIODARONE HYDROCHLORIDE.
Product Information
NDC | 51662-1205 |
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Product ID | 51662-1205_0ef250d9-ba34-8a3e-e063-6394a90acd14 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | AMIODARONE HYDROCHLORIDE |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | AMIODARONE HYDROCHLORIDE |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, SOLUTION |
Route | INTRAVENOUS |
Active Ingredient Strength | 50 |
Active Ingredient Units | mg/mL |
Substance Name | AMIODARONE HYDROCHLORIDE |
Labeler Name | HF Acquisition Co LLC, DBA HealthFirst |
Pharmaceutical Class | Antiarrhythmic [EPC], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA077234 |
Listing Certified Through | 2025-12-31 |
Package
NDC 51662-1205-03 (51662120503)
NDC Package Code | 51662-1205-3 |
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Billing NDC | 51662120503 |
Package | 25 POUCH in 1 CASE (51662-1205-3) / 1 mL in 1 POUCH (51662-1205-2) |
Marketing Start Date | 2020-06-15 |
NDC Exclude Flag | N |
Pricing Information | N/A |