Risperidone

Product NDC
70121-2625
11-digit product format
701212625
Labeler code
70121
Product ID
70121-2625_1109da94-12c2-4378-b9fb-74f94382b90a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
risperidone
Dosage form
KIT
Route
SUBCUTANEOUS
Labeler
Amneal Pharmaceuticals LLC
Application
ANDA218586
Marketing category
ANDA
Marketing start
2025-09-08
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA Listing Details

Product ID
70121-2625_1109da94-12c2-4378-b9fb-74f94382b90a
Product type
HUMAN PRESCRIPTION DRUG
Finished product
Yes
Brand name base
Risperidone
Generic name
risperidone
Dosage form
KIT
Route
SUBCUTANEOUS
Marketing start
2025-09-08
Marketing category
ANDA
Application number
ANDA218586
Listing expiration
2026-12-31

Related Records

openFDA Harmonized Identifiers

FieldValues
Rxcui402010, 402011, 402012, 706822
Spl Set Idd526af85-ee70-4657-a27e-d451027ffd9e
Manufacturer NameAmneal Pharmaceuticals LLC

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
L6UH7ZF8HCRISPERIDONE106266-06-2risperidone

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70121-2625-5701212625051 KIT in 1 CARTON (70121-2625-5) * 2 mL in 1 VIAL (70121-1350-1) * 2 mL in 1 SYRINGE (70121-2624-2) 1 kit2025-09-08NoNoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
RisperidoneAmneal Pharmaceuticals LLC | Amneal Pharmaceuticals Private Limited2025-07-06HUMAN PRESCRIPTION DRUG LABEL6