Package 62135-702-90

Brand: amoxapine

Generic: amoxapine
NDC Package

Package Facts

Identity

Package NDC 62135-702-90
Digits Only 6213570290
Product NDC 62135-702
Product ID 62135-702_298fbb0d-737b-b42f-e063-6394a90ac69b
Description

90 TABLET in 1 BOTTLE (62135-702-90)

Marketing

Marketing Status
Marketed Since 2023-09-06
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": "298fbb0d-737b-b42f-e063-6394a90ac69b", "openfda": {"nui": ["N0000175752"], "upc": ["0362135702908", "0362135701901", "0362135700904", "0362135703301"], "unii": ["R63VQ857OT"], "rxcui": ["197363", "197364", "197365", "197366"], "spl_set_id": ["eed5e856-dd7b-4eaa-9dad-508f2bef9328"], "pharm_class_epc": ["Tricyclic Antidepressant [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-702-90)", "package_ndc": "62135-702-90", "marketing_start_date": "20230906"}], "brand_name": "Amoxapine", "product_id": "62135-702_298fbb0d-737b-b42f-e063-6394a90ac69b", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "62135-702", "generic_name": "Amoxapine", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxapine", "active_ingredients": [{"name": "AMOXAPINE", "strength": "100 mg/1"}], "application_number": "ANDA072879", "marketing_category": "ANDA", "marketing_start_date": "19910628", "listing_expiration_date": "20261231"}