risperidone

Generic: risperidone

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name risperidone
Generic Name risperidone
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

risperidone 1 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-254
Product ID 43063-254_32825602-7abb-8f64-e063-6394a90aadd3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079088
Listing Expiration 2026-12-31
Marketing Start 2009-01-01

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063254
Hyphenated Format 43063-254

Supplemental Identifiers

RxCUI
312830
UPC
0343063254301
UNII
L6UH7ZF8HC
NUI
N0000175430

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 ANDA079088 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-254-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-254-60)
source: ndc

Packages (2)

43063-254-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-254-30) 43063-254-60 60 TABLET in 1 BOTTLE, PLASTIC (43063-254-60)

Ingredients (1)

risperidone (1 mg/1)

Linked Drug Pages (1)

Risperidone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "32825602-7abb-8f64-e063-6394a90aadd3", "openfda": {"nui": ["N0000175430"], "upc": ["0343063254301"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312830"], "spl_set_id": ["e72a2768-815f-47bf-b2f9-16a93dd10684"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-254-30)", "package_ndc": "43063-254-30", "marketing_start_date": "20100603"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-254-60)", "package_ndc": "43063-254-60", "marketing_start_date": "20100603"}], "brand_name": "Risperidone", "product_id": "43063-254_32825602-7abb-8f64-e063-6394a90aadd3", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "43063-254", "generic_name": "Risperidone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risperidone", "active_ingredients": [{"name": "RISPERIDONE", "strength": "1 mg/1"}], "application_number": "ANDA079088", "marketing_category": "ANDA", "marketing_start_date": "20090101", "listing_expiration_date": "20261231"}