Package 63323-751-13

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-751-13
Digits Only 6332375113
Product NDC 63323-751
Product ID 63323-751_34ab57b5-98e6-4284-8f0a-96334a07a915
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (63323-751-13) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-751-03)

Marketing

Marketing Status
Marketed Since 2019-05-25
Brand phenylephrine hydrochloride
Generic phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Phenylephrine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "34ab57b5-98e6-4284-8f0a-96334a07a915", "openfda": {"upc": ["0363323751036"], "unii": ["04JA59TNSJ"], "rxcui": ["1666372"], "spl_set_id": ["f2dce7f1-6538-4747-9792-665eee45c0a9"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (63323-751-13)  / 1 mL in 1 VIAL, SINGLE-DOSE (63323-751-03)", "package_ndc": "63323-751-13", "marketing_start_date": "20190525"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "63323-751_34ab57b5-98e6-4284-8f0a-96334a07a915", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "63323-751", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA210665", "marketing_category": "ANDA", "marketing_start_date": "20190525", "listing_expiration_date": "20261231"}