chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine hydrochloride
Generic Name chlorpromazine hydrochloride
Labeler northstar rx llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 50 mg/1

Manufacturer
Northstar Rx LLC

Identifiers & Regulatory

Product NDC 16714-049
Product ID 16714-049_13fe8f97-37e8-4d10-87fe-e1d17f4f23d8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213368
Listing Expiration 2026-12-31
Marketing Start 2020-05-11

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16714049
Hyphenated Format 16714-049

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
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 ANDA213368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (16714-049-01)
source: ndc

Packages (1)

16714-049-01 100 TABLET, FILM COATED in 1 BOTTLE (16714-049-01)

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": "13fe8f97-37e8-4d10-87fe-e1d17f4f23d8", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["2bd42d3a-bf89-4d74-a252-9b914106a570"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-049-01)", "package_ndc": "16714-049-01", "marketing_start_date": "20200511"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "16714-049_13fe8f97-37e8-4d10-87fe-e1d17f4f23d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "16714-049", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA213368", "marketing_category": "ANDA", "marketing_start_date": "20200511", "listing_expiration_date": "20261231"}