Package 70069-801-25
Brand: phenylephrine hydrochloride
Generic: phenylephrine hydrochloridePackage Facts
Identity
Package NDC
70069-801-25
Digits Only
7006980125
Product NDC
70069-801
Description
25 VIAL in 1 CARTON (70069-801-25) / 1 mL in 1 VIAL (70069-801-01)
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": "90a3853e-49d6-4536-be72-82cc875bcf74", "openfda": {"upc": ["0370069803011", "0370069802014", "0370069801017"], "unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372"], "spl_set_id": ["90a3853e-49d6-4536-be72-82cc875bcf74"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70069-801-25) / 1 mL in 1 VIAL (70069-801-01)", "package_ndc": "70069-801-25", "marketing_start_date": "20210922"}], "brand_name": "PHENYLEPHRINE HYDROCHLORIDE", "product_id": "70069-801_90a3853e-49d6-4536-be72-82cc875bcf74", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "70069-801", "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": "10 mg/mL"}], "application_number": "ANDA213318", "marketing_category": "ANDA", "marketing_start_date": "20210922", "listing_expiration_date": "20261231"}