chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 100 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4294
Product ID 70518-4294_401ccac6-a5d6-bf76-e063-6294a90a87f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084114
Listing Expiration 2026-12-31
Marketing Start 2025-02-26

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184294
Hyphenated Format 70518-4294

Supplemental Identifiers

RxCUI
991044
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 ANDA084114 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 BOX (70518-4294-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4294-1)
source: ndc

Packages (1)

70518-4294-0 100 POUCH in 1 BOX (70518-4294-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4294-1)

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": "401ccac6-a5d6-bf76-e063-6294a90a87f0", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991044"], "spl_set_id": ["9709ffde-7034-42be-97be-f5f39eeacf72"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-4294-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4294-1)", "package_ndc": "70518-4294-0", "marketing_start_date": "20250226"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70518-4294_401ccac6-a5d6-bf76-e063-6294a90a87f0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4294", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA084114", "marketing_category": "ANDA", "marketing_start_date": "20250226", "listing_expiration_date": "20261231"}