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Phenylephrine Hydrochloride
Phenylephrine Hydrochloride - 0517-0299-25 - (Phenylephrine Hydrochloride)
Drug Information of Phenylephrine Hydrochloride
| Product NDC: | 0517-0299 |
| Proprietary Name: | Phenylephrine Hydrochloride |
| Non Proprietary Name: | Phenylephrine Hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; Phenylephrine Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenylephrine Hydrochloride
| Product NDC: | 0517-0299 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900930 |
Package Information of Phenylephrine Hydrochloride
| Package NDC: | 0517-0299-25 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (0517-0299-25) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Phenylephrine Hydrochloride
| NDC Code | 0517-0299-25 |
| Proprietary Name | Phenylephrine Hydrochloride |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0517-0299-25) > 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-0299 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenylephrine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 19900930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
