Package 0781-9228-70
Brand: phenylephrine hydrochloride
Generic: phenylephrine hydrochloridePackage Facts
Identity
Package NDC
0781-9228-70
Digits Only
0781922870
Product NDC
0781-9228
Description
1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-9228-70) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE
Marketing
Marketing Status
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": "eb4076c0-0b18-332f-e053-2a95a90aae13", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372"], "spl_set_id": ["5788f8c6-f868-4b83-81dc-dc485d8716c0"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-9228-70) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "0781-9228-70", "marketing_start_date": "20210217"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "0781-9228_eb4076c0-0b18-332f-e053-2a95a90aae13", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0781-9228", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA208905", "marketing_category": "ANDA", "marketing_start_date": "20210217", "listing_expiration_date": "20261231"}