Package 70069-819-10

Brand: ephedrine sulfate

Generic: ephedrine sulfate
NDC Package

Package Facts

Identity

Package NDC 70069-819-10
Digits Only 7006981910
Product NDC 70069-819
Description

10 VIAL in 1 CARTON (70069-819-10) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-11-07
Brand ephedrine sulfate
Generic ephedrine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "320a0a1f-18e3-4bdb-8856-965f403666ba", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["86b1c42c-854e-463b-ac99-4aacbbe71fd1"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70069-819-10)  / 1 mL in 1 VIAL", "package_ndc": "70069-819-10", "marketing_start_date": "20241107"}], "brand_name": "EPHEDRINE SULFATE", "product_id": "70069-819_320a0a1f-18e3-4bdb-8856-965f403666ba", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Releasing Agent [EPC]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "70069-819", "generic_name": "EPHEDRINE SULFATE", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EPHEDRINE SULFATE", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA216146", "marketing_category": "ANDA", "marketing_start_date": "20241107", "listing_expiration_date": "20261231"}