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NDC 55150-0421-10 esmolol hydrochloride 20 mg/mL Details
esmolol hydrochloride 20 mg/mL
esmolol hydrochloride is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eugia US LLC. The primary component is ESMOLOL HYDROCHLORIDE.
Product Information
| NDC | 55150-0421 |
|---|---|
| Product ID | 55150-421_b6fe7379-bb70-414a-9f92-bba99036ff05 |
| Associated GPIs | 33200025112030 |
| GCN Sequence Number | 052014 |
| GCN Sequence Number Description | esmolol in sodium chloride,iso IV SOLN 2000MG/100 INTRAVEN |
| HIC3 | J7C |
| HIC3 Description | BETA-ADRENERGIC BLOCKING AGENTS |
| GCN | 19503 |
| HICL Sequence Number | 025126 |
| HICL Sequence Number Description | ESMOLOL HCL IN SODIUM CHLORIDE, ISO-OSMOTIC |
| Brand/Generic | Generic |
| Proprietary Name | esmolol hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | esmolol hydrochloride in sodium chloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/mL |
| Substance Name | ESMOLOL HYDROCHLORIDE |
| Labeler Name | Eugia US LLC |
| Pharmaceutical Class | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA216244 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 55150-0421-10 (55150042110)
| NDC Package Code | 55150-421-10 |
|---|---|
| Billing NDC | 55150042110 |
| Package | 10 POUCH in 1 CARTON (55150-421-10) / 1 BAG in 1 POUCH (55150-421-01) / 100 mL in 1 BAG |
| Marketing Start Date | 2022-03-21 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |