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NDC 70121-1637-05 Ephedrine Sulfate 50 mg/mL Details
Ephedrine Sulfate 50 mg/mL
Ephedrine Sulfate is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is EPHEDRINE SULFATE.
Product Information
| NDC | 70121-1637 |
|---|---|
| Product ID | 70121-1637_1fbe12bc-b6af-4cd5-be5c-7e9b305c0970 |
| Associated GPIs | 38000030102015 |
| GCN Sequence Number | 076091 |
| GCN Sequence Number Description | ephedrine sulfate VIAL 50MG/ML(1) INTRAVEN |
| HIC3 | J5E |
| HIC3 Description | SYMPATHOMIMETIC AGENTS |
| GCN | 41364 |
| HICL Sequence Number | 002084 |
| HICL Sequence Number Description | EPHEDRINE SULFATE |
| Brand/Generic | Generic |
| Proprietary Name | Ephedrine Sulfate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ephedrine Sulfate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/mL |
| Substance Name | EPHEDRINE SULFATE |
| Labeler Name | Amneal Pharmaceuticals LLC |
| Pharmaceutical Class | Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA212932 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70121-1637-05 (70121163705)
| NDC Package Code | 70121-1637-5 |
|---|---|
| Billing NDC | 70121163705 |
| Package | 25 VIAL, SINGLE-DOSE in 1 CARTON (70121-1637-5) / 1 mL in 1 VIAL, SINGLE-DOSE (70121-1637-1) |
| Marketing Start Date | 2019-10-23 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |