Package 0527-2964-37

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0527-2964-37
Digits Only 0527296437
Product NDC 0527-2964
Product ID 0527-2964_03738900-0fff-440f-bcaa-ec16f7201f6e
Description

100 TABLET, COATED in 1 BOTTLE (0527-2964-37)

Marketing

Marketing Status
Marketed Since 2021-01-22
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Chlorpromazine Hydrochloride ndc-match (0.95)

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 (0527-2964-37)", "package_ndc": "0527-2964-37", "marketing_start_date": "20210122"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (0527-2964-43)", "package_ndc": "0527-2964-43", "marketing_start_date": "20210122"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "0527-2964_03738900-0fff-440f-bcaa-ec16f7201f6e", "dosage_form": "TABLET, COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0527-2964", "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": "100 mg/1"}], "application_number": "ANDA212996", "marketing_category": "ANDA", "marketing_start_date": "20210122", "listing_expiration_date": "20261231"}