Package 71839-129-10

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71839-129-10
Digits Only 7183912910
Product NDC 71839-129
Product ID 71839-129_fb069778-d16e-40f9-9c02-5496adfcb5d2
Description

10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (71839-129-10) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE (71839-129-01)

Marketing

Marketing Status
Marketed Since 2023-07-10
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": "fb069778-d16e-40f9-9c02-5496adfcb5d2", "openfda": {"upc": ["0371839129010", "0371839127016", "0371839128013"], "unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372"], "spl_set_id": ["fb069778-d16e-40f9-9c02-5496adfcb5d2"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (71839-129-10)  / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE (71839-129-01)", "package_ndc": "71839-129-10", "marketing_start_date": "20230710"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "71839-129_fb069778-d16e-40f9-9c02-5496adfcb5d2", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "71839-129", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA217521", "marketing_category": "ANDA", "marketing_start_date": "20230710", "listing_expiration_date": "20261231"}