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, SUGAR COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3510
Product ID 70518-3510_4c0e03ae-d19e-a44f-e063-6294a90a58bf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214827
Listing Expiration 2027-12-31
Marketing Start 2022-09-06

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183510
Hyphenated Format 70518-3510

Supplemental Identifiers

RxCUI
991194
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 ANDA214827 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3510-0)
source: ndc

Packages (1)

70518-3510-0 30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3510-0)

Ingredients (1)

chlorpromazine hydrochloride (25 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": "4c0e03ae-d19e-a44f-e063-6294a90a58bf", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991194"], "spl_set_id": ["2122d619-3f5b-48f6-8f0b-7693199abbdb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3510-0)", "package_ndc": "70518-3510-0", "marketing_start_date": "20220906"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70518-3510_4c0e03ae-d19e-a44f-e063-6294a90a58bf", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3510", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA214827", "marketing_category": "ANDA", "marketing_start_date": "20220906", "listing_expiration_date": "20271231"}