Package 0781-3269-95

Brand: ephedrine sulfate

Generic: ephedrine sulfate
NDC Package

Package Facts

Identity

Package NDC 0781-3269-95
Digits Only 0781326995
Product NDC 0781-3269
Product ID 0781-3269_f923276f-a7dd-4940-9544-a71525cd5e1c
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3269-95) / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3269-71)

Marketing

Marketing Status
Marketed Since 2017-10-01
Brand ephedrine sulfate
Generic ephedrine sulfate
Sample Package No

Linked Drug Pages (1)

Ephedrine Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "f923276f-a7dd-4940-9544-a71525cd5e1c", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["c8af7bb5-41da-4f8c-8acd-f489892a0d72"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3269-95)  / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3269-71)", "package_ndc": "0781-3269-95", "marketing_start_date": "20171001"}], "brand_name": "Ephedrine Sulfate", "product_id": "0781-3269_f923276f-a7dd-4940-9544-a71525cd5e1c", "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": "0781-3269", "generic_name": "Ephedrine Sulfate", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ephedrine Sulfate", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA209784", "marketing_category": "ANDA", "marketing_start_date": "20171001", "listing_expiration_date": "20261231"}