chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

chlorpromazine hydrochloride 50 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-2963
Product ID 0527-2963_03738900-0fff-440f-bcaa-ec16f7201f6e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212996
Listing Expiration 2026-12-31
Marketing Start 2021-01-22

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05272963
Hyphenated Format 0527-2963

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0305272962378
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 ANDA212996 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (0527-2963-37)
  • 1000 TABLET, COATED in 1 BOTTLE (0527-2963-43)
source: ndc

Packages (2)

0527-2963-37 100 TABLET, COATED in 1 BOTTLE (0527-2963-37) 0527-2963-43 1000 TABLET, COATED in 1 BOTTLE (0527-2963-43)

Ingredients (1)

chlorpromazine hydrochloride (50 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": "03738900-0fff-440f-bcaa-ec16f7201f6e", "openfda": {"upc": ["0305272962378"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["1049538a-c012-41bf-932e-3c85f57f9577"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (0527-2963-37)", "package_ndc": "0527-2963-37", "marketing_start_date": "20210122"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (0527-2963-43)", "package_ndc": "0527-2963-43", "marketing_start_date": "20210122"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "0527-2963_03738900-0fff-440f-bcaa-ec16f7201f6e", "dosage_form": "TABLET, COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0527-2963", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA212996", "marketing_category": "ANDA", "marketing_start_date": "20210122", "listing_expiration_date": "20261231"}