Paliperidone
These highlights do not include all the information needed to use PALIPERIDONE EXTENDED-RELEASE TABLETS safely and effectively. See full prescribing information for PALIPERIDONE EXTENDED-RELEASE TABLETS. PALIPERIDONE extended-release tablets, for oral use Initial U.S. Approval: 2006
0dc3a9b2-2edf-4fa2-a949-459b4218e763
HUMAN PRESCRIPTION DRUG LABEL
Oct 25, 2023
Sun Pharmaceutical Industries, Inc.
DUNS: 146974886
Products 4
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Paliperidone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
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INGREDIENTS (17)
Paliperidone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
Product Classification
Product Specifications
INGREDIENTS (16)
Paliperidone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
Product Classification
Product Specifications
INGREDIENTS (17)
Paliperidone
Product Details
FDA regulatory identification and product classification information