chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler upsher-smith laboratories, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 50 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 0832-6019
Product ID 0832-6019_787f32b3-e4f6-424d-a2c0-d249b5bbcd93
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084113
Listing Expiration 2027-12-31
Marketing Start 2011-08-03

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 08326019
Hyphenated Format 0832-6019

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0308326020000 0308326018007 0308326021007 0308326017000 0308326019004
UNII
9WP59609J6

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name chlorpromazine hydrochloride (source: ndc)
Generic Name chlorpromazine hydrochloride (source: ndc)
Application Number ANDA084113 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0832-6019-00)
  • 1 BLISTER PACK in 1 CARTON (0832-6019-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6019-89)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (0832-6019-10)
source: ndc

Packages (3)

0832-6019-00 100 TABLET, FILM COATED in 1 BOTTLE (0832-6019-00) 0832-6019-01 1 BLISTER PACK in 1 CARTON (0832-6019-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6019-89) 0832-6019-10 1000 TABLET, FILM COATED in 1 BOTTLE (0832-6019-10)

Ingredients (1)

chlorpromazine hydrochloride (50 mg/1)

Linked Drug Pages (1)

Chlorpromazine Hydrochloride ndc-match (0.9)

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 (0832-6019-00)", "package_ndc": "0832-6019-00", "marketing_start_date": "20210806"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0832-6019-01)  / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6019-89)", "package_ndc": "0832-6019-01", "marketing_start_date": "20210806"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0832-6019-10)", "package_ndc": "0832-6019-10", "marketing_start_date": "20210806"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "0832-6019_787f32b3-e4f6-424d-a2c0-d249b5bbcd93", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0832-6019", "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": "50 mg/1"}], "application_number": "ANDA084113", "marketing_category": "ANDA", "marketing_start_date": "20110803", "listing_expiration_date": "20271231"}