Package 72603-181-01

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 72603-181-01
Digits Only 7260318101
Product NDC 72603-181
Description

1 VIAL in 1 CARTON (72603-181-01) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-10-16
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "075ca296-d5cc-1898-e063-6394a90acd13", "openfda": {"nui": ["N0000175430"], "upc": ["0372603181012"], "unii": ["N7U69T4SZR"], "rxcui": ["485968"], "spl_set_id": ["f4e41c2c-d32d-40c2-8afb-b6df998ba6b0"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (72603-181-01)  / 2 mL in 1 VIAL", "package_ndc": "72603-181-01", "marketing_start_date": "20231016"}], "brand_name": "Olanzapine", "product_id": "72603-181_075ca296-d5cc-1898-e063-6394a90acd13", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72603-181", "generic_name": "Olanzapine", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/2mL"}], "application_number": "ANDA217466", "marketing_category": "ANDA", "marketing_start_date": "20231016", "listing_expiration_date": "20261231"}