Package 71610-419-30

Brand: olanzapine

Generic: olanzapine
NDC Package

Package Facts

Identity

Package NDC 71610-419-30
Digits Only 7161041930
Product NDC 71610-419
Product ID 71610-419_de72ce02-c9dd-4462-aca5-87fb4427c78a
Description

30 TABLET, FILM COATED in 1 BOTTLE (71610-419-30)

Marketing

Marketing Status
Marketed Since 2020-04-23
Brand olanzapine
Generic olanzapine
Sample Package No

Linked Drug Pages (1)

Olanzapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "de72ce02-c9dd-4462-aca5-87fb4427c78a", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312077"], "spl_set_id": ["b6ec5610-b4a6-4646-954a-0fe8b1d3e143"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-419-30)", "package_ndc": "71610-419-30", "marketing_start_date": "20200423"}], "brand_name": "Olanzapine", "product_id": "71610-419_de72ce02-c9dd-4462-aca5-87fb4427c78a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71610-419", "generic_name": "Olanzapine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "15 mg/1"}], "application_number": "ANDA090798", "marketing_category": "ANDA", "marketing_start_date": "20120423", "listing_expiration_date": "20261231"}