Package 0904-7362-61

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 0904-7362-61
Digits Only 0904736261
Product NDC 0904-7362
Description

100 BLISTER PACK in 1 CARTON (0904-7362-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-10-27
Brand risperidone
Generic risperidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41d98aaf-a69e-414d-af3f-2c815cd1f43a", "openfda": {"nui": ["N0000175430"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312828", "312829", "312830", "312831", "312832", "314211"], "spl_set_id": ["d5abd75f-7f4a-4a7d-b849-82fce88f5ff7"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7362-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7362-61", "marketing_start_date": "20231027"}], "brand_name": "risperidone", "product_id": "0904-7362_41d98aaf-a69e-414d-af3f-2c815cd1f43a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-7362", "generic_name": "risperidone", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "risperidone", "active_ingredients": [{"name": "RISPERIDONE", "strength": "1 mg/1"}], "application_number": "ANDA078040", "marketing_category": "ANDA", "marketing_start_date": "20081113", "listing_expiration_date": "20271231"}