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NDC 65219-0140-04 Norepinephrine Bitartrate 1 mg/mL Details
Norepinephrine Bitartrate 1 mg/mL
Norepinephrine Bitartrate is a INTRAVENOUS SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Fresenius Kabi USA, LLC. The primary component is NOREPINEPHRINE BITARTRATE.
Product Information
| NDC | 65219-0140 |
|---|---|
| Product ID | 65219-140_6ccb3099-bd2e-44f5-9585-031ab620e640 |
| Associated GPIs | |
| GCN Sequence Number | 028633 |
| GCN Sequence Number Description | norepinephrine bitartrate VIAL 1 MG/ML INTRAVEN |
| HIC3 | J5A |
| HIC3 Description | ADRENERGIC AGENTS,CATECHOLAMINES |
| GCN | 00476 |
| HICL Sequence Number | 002051 |
| HICL Sequence Number Description | NOREPINEPHRINE BITARTRATE |
| Brand/Generic | Generic |
| Proprietary Name | Norepinephrine Bitartrate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | NOREPINEPHRINE BITARTRATE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | mg/mL |
| Substance Name | NOREPINEPHRINE BITARTRATE |
| Labeler Name | Fresenius Kabi USA, LLC |
| Pharmaceutical Class | Catecholamine [EPC], Catecholamines [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA211382 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65219-0140-04 (65219014004)
| NDC Package Code | 65219-140-04 |
|---|---|
| Billing NDC | 65219014004 |
| Package | 10 VIAL, SINGLE-DOSE in 1 CARTON (65219-140-04) / 4 mL in 1 VIAL, SINGLE-DOSE (65219-140-02) |
| Marketing Start Date | 2021-03-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |