risperidone
Generic: risperidone
Labeler: nucare pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
risperidone
Generic Name
risperidone
Labeler
nucare pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
risperidone 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3873
Product ID
68071-3873_390901b0-fcfa-47cd-e063-6294a90a3c2d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077493
Listing Expiration
2026-12-31
Marketing Start
2014-06-01
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713873
Hyphenated Format
68071-3873
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA077493 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (68071-3873-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "390901b0-fcfa-47cd-e063-6294a90a3c2d", "openfda": {"nui": ["N0000175430"], "upc": ["0368071387339"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312830"], "spl_set_id": ["390904c2-fcfa-466e-e063-6394a90a03af"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3873-3)", "package_ndc": "68071-3873-3", "marketing_start_date": "20250703"}], "brand_name": "Risperidone", "product_id": "68071-3873_390901b0-fcfa-47cd-e063-6294a90a3c2d", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3873", "generic_name": "Risperidone", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risperidone", "active_ingredients": [{"name": "RISPERIDONE", "strength": "1 mg/1"}], "application_number": "ANDA077493", "marketing_category": "ANDA", "marketing_start_date": "20140601", "listing_expiration_date": "20261231"}