chlorpromazine

Generic: chlorpromazine

Labeler: alembic pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name chlorpromazine
Generic Name chlorpromazine
Labeler alembic pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

chlorpromazine hydrochloride 100 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-738
Product ID 46708-738_1f9751ff-33da-44be-9c1f-9bbf88ac543b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217350
Listing Expiration 2026-12-31
Marketing Start 2023-07-20

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46708738
Hyphenated Format 46708-738

Supplemental Identifiers

RxCUI
991039 991044 991188 991194 991336
UPC
0346708736316 0346708737313 0346708735319 0346708738310
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 (source: ndc)
Generic Name chlorpromazine (source: ndc)
Application Number ANDA217350 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (46708-738-10) / 10 TABLET in 1 BLISTER PACK
  • 100 TABLET in 1 BOTTLE (46708-738-31)
  • 1000 TABLET in 1 BOTTLE (46708-738-91)
source: ndc

Packages (3)

46708-738-10 100 BLISTER PACK in 1 CARTON (46708-738-10) / 10 TABLET in 1 BLISTER PACK 46708-738-31 100 TABLET in 1 BOTTLE (46708-738-31) 46708-738-91 1000 TABLET in 1 BOTTLE (46708-738-91)

Ingredients (1)

chlorpromazine hydrochloride (100 mg/1)

Linked Drug Pages (1)

Chlorpromazine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1f9751ff-33da-44be-9c1f-9bbf88ac543b", "openfda": {"upc": ["0346708736316", "0346708737313", "0346708735319", "0346708738310"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["1f9751ff-33da-44be-9c1f-9bbf88ac543b"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (46708-738-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "46708-738-10", "marketing_start_date": "20230720"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (46708-738-31)", "package_ndc": "46708-738-31", "marketing_start_date": "20230720"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-738-91)", "package_ndc": "46708-738-91", "marketing_start_date": "20230720"}], "brand_name": "Chlorpromazine", "product_id": "46708-738_1f9751ff-33da-44be-9c1f-9bbf88ac543b", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "46708-738", "generic_name": "Chlorpromazine", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA217350", "marketing_category": "ANDA", "marketing_start_date": "20230720", "listing_expiration_date": "20261231"}