chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 25 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-430
Product ID 60687-430_4342f33e-4430-7a74-e063-6294a90adba7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209755
Listing Expiration 2026-12-31
Marketing Start 2019-05-16

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687430
Hyphenated Format 60687-430

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UNII
9WP59609J6

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 ANDA209755 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-430-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-430-11)
  • 50 BLISTER PACK in 1 CARTON (60687-430-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-430-11)
source: ndc

Packages (2)

60687-430-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-430-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-430-11) 60687-430-65 50 BLISTER PACK in 1 CARTON (60687-430-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-430-11)

Ingredients (1)

chlorpromazine hydrochloride (25 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": "4342f33e-4430-7a74-e063-6294a90adba7", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["d43718e5-66d7-44f9-9fc8-80d38d3e41ce"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-430-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-430-11)", "package_ndc": "60687-430-01", "marketing_end_date": "20270731", "marketing_start_date": "20190516"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (60687-430-65)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-430-11)", "package_ndc": "60687-430-65", "marketing_start_date": "20240728"}], "brand_name": "CHLORPROMAZINE HYDROCHLORIDE", "product_id": "60687-430_4342f33e-4430-7a74-e063-6294a90adba7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "60687-430", "generic_name": "CHLORPROMAZINE HYDROCHLORIDE", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORPROMAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA209755", "marketing_category": "ANDA", "marketing_start_date": "20190516", "listing_expiration_date": "20261231"}