Package 0591-5716-30

Brand: amoxapine

Generic: amoxapine
NDC Package

Package Facts

Identity

Package NDC 0591-5716-30
Digits Only 0591571630
Product NDC 0591-5716
Product ID 0591-5716_40931661-1155-4850-baaa-227f066ed616
Description

30 TABLET in 1 BOTTLE, PLASTIC (0591-5716-30)

Marketing

Marketing Status
Marketed Since 1992-08-28
Brand amoxapine
Generic amoxapine
Sample Package No

Linked Drug Pages (1)

Amoxapine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40931661-1155-4850-baaa-227f066ed616", "openfda": {"nui": ["N0000175752"], "unii": ["R63VQ857OT"], "rxcui": ["197363", "197364", "197365", "197366"], "spl_set_id": ["a16297df-3158-48db-85e5-5cd506885556"], "pharm_class_epc": ["Tricyclic Antidepressant [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (0591-5716-30)", "package_ndc": "0591-5716-30", "marketing_start_date": "19920828"}], "brand_name": "Amoxapine", "product_id": "0591-5716_40931661-1155-4850-baaa-227f066ed616", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0591-5716", "generic_name": "Amoxapine", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxapine", "active_ingredients": [{"name": "AMOXAPINE", "strength": "150 mg/1"}], "application_number": "ANDA072691", "marketing_category": "ANDA", "marketing_start_date": "19920828", "listing_expiration_date": "20271231"}