Package 70069-812-10

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-812-10
Digits Only 7006981210
Product NDC 70069-812
Product ID 70069-812_18b65b44-fdd1-4385-b6f8-cf3cbdc8d0e6
Description

10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70069-812-10) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (70069-812-01)

Marketing

Marketing Status
Marketed Since 2023-07-17
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": "18b65b44-fdd1-4385-b6f8-cf3cbdc8d0e6", "openfda": {"upc": ["0370069813010"], "unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372"], "spl_set_id": ["18b65b44-fdd1-4385-b6f8-cf3cbdc8d0e6"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (70069-812-10)  / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (70069-812-01)", "package_ndc": "70069-812-10", "marketing_start_date": "20230717"}], "brand_name": "PHENYLEPHRINE HYDROCHLORIDE", "product_id": "70069-812_18b65b44-fdd1-4385-b6f8-cf3cbdc8d0e6", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "70069-812", "generic_name": "PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENYLEPHRINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "50 mg/5mL"}], "application_number": "ANDA213318", "marketing_category": "ANDA", "marketing_start_date": "20230717", "listing_expiration_date": "20261231"}