Package 70710-1133-4
Brand: chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloridePackage Facts
Identity
Package NDC
70710-1133-4
Digits Only
7071011334
Product NDC
70710-1133
Description
10 BLISTER PACK in 1 CARTON (70710-1133-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1133-2)
Marketing
Marketing Status
Brand
chlorpromazine hydrochloride
Generic
chlorpromazine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8a5df7d8-ad17-44d7-9c56-44fa2aaa0852", "openfda": {"upc": ["0370710112912", "0370710113216", "0370710113018"], "unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["fc2bd95d-a7bc-4ab5-bffa-f5059cb8eb63"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1133-1)", "package_ndc": "70710-1133-1", "marketing_start_date": "20200127"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70710-1133-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1133-2)", "package_ndc": "70710-1133-4", "marketing_start_date": "20200127"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "70710-1133_8a5df7d8-ad17-44d7-9c56-44fa2aaa0852", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70710-1133", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA213368", "marketing_category": "ANDA", "marketing_start_date": "20200127", "listing_expiration_date": "20261231"}