Package 68071-3669-9

Brand: imipramine hydrochloride

Generic: imipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3669-9
Digits Only 6807136699
Product NDC 68071-3669
Product ID 68071-3669_209ca50a-3b5e-3799-e063-6294a90a80e4
Description

90 TABLET in 1 BOTTLE (68071-3669-9)

Marketing

Marketing Status
Marketed Since 2020-08-01
Brand imipramine hydrochloride
Generic imipramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Imipramine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "209ca50a-3b5e-3799-e063-6294a90a80e4", "openfda": {"upc": ["0368071366990"], "unii": ["BKE5Q1J60U"], "rxcui": ["835568"], "spl_set_id": ["209cc339-658a-577a-e063-6394a90a2b47"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3669-9)", "package_ndc": "68071-3669-9", "marketing_start_date": "20200801"}], "brand_name": "Imipramine Hydrochloride", "product_id": "68071-3669_209ca50a-3b5e-3799-e063-6294a90a80e4", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68071-3669", "generic_name": "Imipramine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Imipramine Hydrochloride", "active_ingredients": [{"name": "IMIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040751", "marketing_category": "ANDA", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}