chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler zydus lifesciences limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 100 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1509
Product ID 70771-1509_bea6994f-8f72-4c2d-8ba3-c74b10f8412d
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 707711509
Hyphenated Format 70771-1509

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0370771150618 0370771150816 0370771151011 0370771150915
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
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (70771-1509-1)
  • 10 BLISTER PACK in 1 CARTON (70771-1509-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1509-2)
source: ndc

Packages (2)

70771-1509-1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1509-1) 70771-1509-4 10 BLISTER PACK in 1 CARTON (70771-1509-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1509-2)

Ingredients (1)

chlorpromazine hydrochloride (100 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": "bea6994f-8f72-4c2d-8ba3-c74b10f8412d", "openfda": {"upc": ["0370771150618", "0370771150816", "0370771151011", "0370771150915"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["0ea5e0c6-0062-4be3-96f2-62397da3e77d"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1509-1)", "package_ndc": "70771-1509-1", "marketing_start_date": "20200127"}, {"sample": true, "description": "10 BLISTER PACK in 1 CARTON (70771-1509-4)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1509-2)", "package_ndc": "70771-1509-4", "marketing_start_date": "20200127"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "70771-1509_bea6994f-8f72-4c2d-8ba3-c74b10f8412d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70771-1509", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA213368", "marketing_category": "ANDA", "marketing_start_date": "20200127", "listing_expiration_date": "20261231"}