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NDC 23155-0620-41 phenylephrine hydrochloride 10 mg/mL Details
phenylephrine hydrochloride 10 mg/mL
phenylephrine hydrochloride is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. The primary component is PHENYLEPHRINE HYDROCHLORIDE.
Product Information
| NDC | 23155-0620 |
|---|---|
| Product ID | 23155-620_8896d9c7-acf3-4f1f-9632-e1db41a9d5d7 |
| Associated GPIs | |
| GCN Sequence Number | 005068 |
| GCN Sequence Number Description | phenylephrine HCl VIAL 10 MG/ML INJECTION |
| HIC3 | J5E |
| HIC3 Description | SYMPATHOMIMETIC AGENTS |
| GCN | 20310 |
| HICL Sequence Number | 002087 |
| HICL Sequence Number Description | PHENYLEPHRINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | phenylephrine hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | phenylephrine hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/mL |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Labeler Name | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
| Pharmaceutical Class | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA209968 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 23155-0620-41 (23155062041)
| NDC Package Code | 23155-620-41 |
|---|---|
| Billing NDC | 23155062041 |
| Package | 25 VIAL in 1 CARTON (23155-620-41) / 1 mL in 1 VIAL (23155-620-31) |
| Marketing Start Date | 2023-02-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |