| NDC Code | 42023-213-25 | 
|---|
			| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (42023-213-25)  > 1 mL in 1 VIAL, SINGLE-DOSE | 
|---|
			| Product NDC | 42023-213 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Phenylephrine Hydrochloride | 
|---|
			
			| Non-Proprietary Name | Phenylephrine Hydrochloride | 
|---|
			| Dosage Form | INJECTION | 
|---|
			| Usage | INTRAVENOUS | 
|---|
			| Start Marketing Date | 20190717 | 
|---|
			| End Marketing Date | 20220131 | 
|---|
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA210025 | 
|---|
			| Manufacturer | Par Pharmaceutical, Inc. | 
|---|
			| Substance Name | PHENYLEPHRINE HYDROCHLORIDE | 
|---|
			| Strength | 10 | 
|---|
			| Strength Unit | mg/mL | 
|---|
			| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC] | 
|---|