Package 84549-611-25

Brand: ephedrine sulfate

Generic: ephedrine sulfate
NDC Package

Package Facts

Identity

Package NDC 84549-611-25
Digits Only 8454961125
Product NDC 84549-611
Description

1 mL in 1 VIAL, SINGLE-DOSE (84549-611-25)

Marketing

Marketing Status
Marketed Since 2025-08-27
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": "3a38b027-e8ea-5d08-e063-6294a90a3b49", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["3843c820-f54b-5349-e063-6294a90a6b18"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (84549-611-25)", "package_ndc": "84549-611-25", "marketing_start_date": "20250827"}], "brand_name": "Ephedrine sulfate", "product_id": "84549-611_3a38b027-e8ea-5d08-e063-6294a90a3b49", "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": "84549-611", "generic_name": "Ephedrine sulfate", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ephedrine sulfate", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA216129", "marketing_category": "ANDA", "marketing_start_date": "20220415", "listing_expiration_date": "20261231"}