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 INJECTION
Routes
INTRAMUSCULAR
Active Ingredients

chlorpromazine hydrochloride 25 mg/mL

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1778
Product ID 70771-1778_bdfa9437-bd3f-496f-a640-753422d69c85
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217275
Listing Expiration 2026-12-31
Marketing Start 2024-03-29

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711778
Hyphenated Format 70771-1778

Supplemental Identifiers

RxCUI
1730076 1730078
UPC
0370710184971
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 ANDA217275 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (70771-1778-7) / 1 mL in 1 VIAL (70771-1778-1)
source: ndc

Packages (1)

Ingredients (1)

chlorpromazine hydrochloride (25 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "bdfa9437-bd3f-496f-a640-753422d69c85", "openfda": {"upc": ["0370710184971"], "unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["d37a4c21-b503-4791-a4d0-2ccc8891d88e"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70771-1778-7)  / 1 mL in 1 VIAL (70771-1778-1)", "package_ndc": "70771-1778-7", "marketing_start_date": "20240329"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70771-1778_bdfa9437-bd3f-496f-a640-753422d69c85", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70771-1778", "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": "25 mg/mL"}], "application_number": "ANDA217275", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}