Package 0378-0612-01
Brand: thioridazine hydrochloride
Generic: thioridazine hydrochloridePackage Facts
Identity
Package NDC
0378-0612-01
Digits Only
0378061201
Product NDC
0378-0612
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0612-01)
Marketing
Marketing Status
Brand
thioridazine hydrochloride
Generic
thioridazine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6437f615-1e2b-4d0a-ba83-a0c14391693d", "openfda": {"upc": ["0303780618015", "0303780616011", "0303780612013", "0303780614017"], "unii": ["4WCI67NK8M"], "rxcui": ["198270", "198274", "198275", "313354"], "spl_set_id": ["56b3f4c2-52af-4947-b225-6808ae9f26f5"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0612-01)", "package_ndc": "0378-0612-01", "marketing_start_date": "19830315"}], "brand_name": "Thioridazine Hydrochloride", "product_id": "0378-0612_6437f615-1e2b-4d0a-ba83-a0c14391693d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0378-0612", "generic_name": "thioridazine hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thioridazine Hydrochloride", "active_ingredients": [{"name": "THIORIDAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088004", "marketing_category": "ANDA", "marketing_start_date": "19830315", "listing_expiration_date": "20261231"}