Package 0404-9931-99

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9931-99
Digits Only 0404993199
Product NDC 0404-9931
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9931-99) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-01-13
Brand phenylephrine hydrochloride
Generic phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a4ecb606-abf4-4f16-9c91-13d33831033c", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1666372"], "spl_set_id": ["db313f72-a6bb-444f-949f-19b4aa6f61c0"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9931-99)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9931-99", "marketing_start_date": "20220113"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "0404-9931_a4ecb606-abf4-4f16-9c91-13d33831033c", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0404-9931", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA211079", "marketing_category": "ANDA", "marketing_start_date": "20220113", "listing_expiration_date": "20261231"}