Package 62135-593-12

Brand: desipramine hydrochloride

Generic: desipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-593-12
Digits Only 6213559312
Product NDC 62135-593
Description

120 TABLET in 1 BOTTLE (62135-593-12)

Marketing

Marketing Status
Marketed Since 2023-05-12
Brand desipramine hydrochloride
Generic desipramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45895d97-14b1-1beb-e063-6394a90a2930", "openfda": {"upc": ["0362135599300", "0362135593124", "0362135597122", "0362135598303", "0362135594121", "0362135595128"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["6ab5e113-82ef-493d-a4e3-a2756608fa60"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (62135-593-12)", "package_ndc": "62135-593-12", "marketing_start_date": "20230512"}], "brand_name": "Desipramine Hydrochloride", "product_id": "62135-593_45895d97-14b1-1beb-e063-6394a90a2930", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "62135-593", "generic_name": "Desipramine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desipramine Hydrochloride", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207433", "marketing_category": "ANDA", "marketing_start_date": "20161101", "listing_expiration_date": "20261231"}