Package 0904-7039-07

Brand: clomipramine hydrochloride

Generic: clomipramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7039-07
Digits Only 0904703907
Product NDC 0904-7039
Product ID 0904-7039_b7641ab7-974c-4814-97ba-44cf2ca7e10f
Description

30 BLISTER PACK in 1 CARTON (0904-7039-07) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 1996-12-31
Brand clomipramine hydrochloride
Generic clomipramine hydrochloride
Sample Package No

Linked Drug Pages (1)

CLOMIPRAMINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b7641ab7-974c-4814-97ba-44cf2ca7e10f", "openfda": {"unii": ["2LXW0L6GWJ"], "rxcui": ["857297", "857301"], "spl_set_id": ["eff91018-5a5e-4426-96ae-71ecd82273b7"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7039-07)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7039-07", "marketing_start_date": "19961231"}], "brand_name": "CLOMIPRAMINE HYDROCHLORIDE", "product_id": "0904-7039_b7641ab7-974c-4814-97ba-44cf2ca7e10f", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "0904-7039", "generic_name": "Clomipramine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLOMIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "CLOMIPRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA074694", "marketing_category": "ANDA", "marketing_start_date": "19961231", "listing_expiration_date": "20261231"}