chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: zydus pharmaceuticals (usa) inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler zydus pharmaceuticals (usa) inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 50 mg/1

Manufacturer
Zydus Pharmaceuticals (USA) Inc.

Identifiers & Regulatory

Product NDC 70710-1131
Product ID 70710-1131_8a5df7d8-ad17-44d7-9c56-44fa2aaa0852
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213368
Listing Expiration 2026-12-31
Marketing Start 2020-01-27

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101131
Hyphenated Format 70710-1131

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0370710112912 0370710113216 0370710113018
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 ANDA213368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (70710-1131-1)
  • 10 BLISTER PACK in 1 CARTON (70710-1131-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1131-2)
source: ndc

Packages (2)

70710-1131-1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1131-1) 70710-1131-4 10 BLISTER PACK in 1 CARTON (70710-1131-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1131-2)

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": "8a5df7d8-ad17-44d7-9c56-44fa2aaa0852", "openfda": {"upc": ["0370710112912", "0370710113216", "0370710113018"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["fc2bd95d-a7bc-4ab5-bffa-f5059cb8eb63"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1131-1)", "package_ndc": "70710-1131-1", "marketing_start_date": "20200127"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70710-1131-4)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1131-2)", "package_ndc": "70710-1131-4", "marketing_start_date": "20200127"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "70710-1131_8a5df7d8-ad17-44d7-9c56-44fa2aaa0852", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70710-1131", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA213368", "marketing_category": "ANDA", "marketing_start_date": "20200127", "listing_expiration_date": "20261231"}