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Phenylephrine Hydrochloride
Phenylephrine Hydrochloride - 66758-016-04 - (Phenylephrine Hydrochloride)
Drug Information of Phenylephrine Hydrochloride
| Product NDC: | 66758-016 |
| 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: | 66758-016 |
| Labeler Name: | Sandoz Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20050625 |
Package Information of Phenylephrine Hydrochloride
| Package NDC: | 66758-016-04 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 CARTON (66758-016-04) > 5 mL in 1 VIAL, SINGLE-DOSE (66758-016-03) |
NDC Information of Phenylephrine Hydrochloride
| NDC Code | 66758-016-04 |
| Proprietary Name | Phenylephrine Hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (66758-016-04) > 5 mL in 1 VIAL, SINGLE-DOSE (66758-016-03) |
| Product NDC | 66758-016 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenylephrine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20050625 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Sandoz Inc. |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
