risperidone
Generic: risperidone
Labeler: jubilant cadista pharmacuticals inc.Drug Facts
Product Profile
Brand Name
risperidone
Generic Name
risperidone
Labeler
jubilant cadista pharmacuticals inc.
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
risperidone 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59746-020
Product ID
59746-020_90b80768-87f7-4fb1-8142-909dba9555e2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090839
Listing Expiration
2026-12-31
Marketing Start
2011-11-04
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59746020
Hyphenated Format
59746-020
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
risperidone (source: ndc)
Generic Name
risperidone (source: ndc)
Application Number
ANDA090839 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 7 BLISTER PACK in 1 CARTON (59746-020-22) / 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
- 3 BLISTER PACK in 1 CARTON (59746-020-32) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "90b80768-87f7-4fb1-8142-909dba9555e2", "openfda": {"nui": ["N0000175430"], "upc": ["0359746020224", "0359746030223", "0359746010324", "0359746040222", "0359746050221"], "unii": ["L6UH7ZF8HC"], "rxcui": ["401953", "401954", "403825", "616698", "616705"], "spl_set_id": ["739dcf8a-ed73-5eb0-899b-7e51cb73c335"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Jubilant Cadista Pharmacuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 BLISTER PACK in 1 CARTON (59746-020-22) / 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "59746-020-22", "marketing_start_date": "20111104"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (59746-020-32) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "59746-020-32", "marketing_start_date": "20111104"}], "brand_name": "Risperidone", "product_id": "59746-020_90b80768-87f7-4fb1-8142-909dba9555e2", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "59746-020", "generic_name": "Risperidone", "labeler_name": "Jubilant Cadista Pharmacuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risperidone", "active_ingredients": [{"name": "RISPERIDONE", "strength": "1 mg/1"}], "application_number": "ANDA090839", "marketing_category": "ANDA", "marketing_start_date": "20111104", "listing_expiration_date": "20261231"}