Package 0832-6018-10

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0832-6018-10
Digits Only 0832601810
Product NDC 0832-6018
Product ID 0832-6018_787f32b3-e4f6-424d-a2c0-d249b5bbcd93
Description

1000 TABLET, FILM COATED in 1 BOTTLE (0832-6018-10)

Marketing

Marketing Status
Marketed Since 2021-08-06
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Chlorpromazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "787f32b3-e4f6-424d-a2c0-d249b5bbcd93", "openfda": {"upc": ["0308326020000", "0308326018007", "0308326021007", "0308326017000", "0308326019004"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["5ae79c1e-f523-4358-9f8b-7382a03d59bc"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0832-6018-00)", "package_ndc": "0832-6018-00", "marketing_start_date": "20210806"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0832-6018-10)", "package_ndc": "0832-6018-10", "marketing_start_date": "20210806"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "0832-6018_787f32b3-e4f6-424d-a2c0-d249b5bbcd93", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0832-6018", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA084112", "marketing_category": "ANDA", "marketing_start_date": "20110803", "listing_expiration_date": "20271231"}