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NDC 63323-0751-13 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 Fresenius Kabi USA, LLC. The primary component is PHENYLEPHRINE HYDROCHLORIDE.
Product Information
| NDC | 63323-0751 |
|---|---|
| Product ID | 63323-751_f7ea538e-7b2e-4951-967b-27bc594566e9 |
| Associated GPIs | 38000095102020 |
| 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 | Fresenius Kabi USA, LLC |
| Pharmaceutical Class | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA210665 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 63323-0751-13 (63323075113)
| NDC Package Code | 63323-751-13 |
|---|---|
| Billing NDC | 63323075113 |
| Package | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-751-13) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-751-03) |
| Marketing Start Date | 2019-05-25 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |