chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloride
Labeler: zydus pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
chlorpromazine hydrochloride
Generic Name
chlorpromazine hydrochloride
Labeler
zydus pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
chlorpromazine hydrochloride 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70710-1850
Product ID
70710-1850_97106093-2f0a-4cc9-b580-942b015c6c5b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217275
Listing Expiration
2026-12-31
Marketing Start
2024-03-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707101850
Hyphenated Format
70710-1850
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 25 VIAL in 1 CARTON (70710-1850-7) / 2 mL in 1 VIAL (70710-1850-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "97106093-2f0a-4cc9-b580-942b015c6c5b", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["7cd6dc0d-e98d-40ae-80d4-c15f63056abf"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70710-1850-7) / 2 mL in 1 VIAL (70710-1850-1)", "package_ndc": "70710-1850-7", "marketing_start_date": "20240329"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70710-1850_97106093-2f0a-4cc9-b580-942b015c6c5b", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70710-1850", "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": "25 mg/mL"}], "application_number": "ANDA217275", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}