RIVAROXABAN

Product NDC
62332-348
11-digit product format
623320348
Labeler code
62332
Product ID
62332-348_43438909-74d8-4b11-b947-00d06de77c88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
RIVAROXABAN
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Alembic Pharmaceuticals Inc.
Application
ANDA210301
Marketing category
ANDA
Marketing start
2025-05-14
Substance
RIVAROXABAN
Active strength
20 mg/1
Pharmacologic classes
Factor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
9NDF7JZ4M3RIVAROXABAN366789-02-8RIVAROXABAN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62332-348-1062332034810100 BLISTER PACK in 1 CARTON (62332-348-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK100 blister pack2025-05-14NoNoHistorical
62332-348-306233203483030 TABLET, FILM COATED in 1 BOTTLE (62332-348-30) 2025-05-14NoNoHistorical
62332-348-906233203489090 TABLET, FILM COATED in 1 BOTTLE (62332-348-90) 2025-05-14NoNoHistorical
62332-348-91623320348911000 TABLET, FILM COATED in 1 BOTTLE (62332-348-91) 2025-05-14NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
RIVAROXABANAlembic Pharmaceuticals Inc. | Alembic Pharmaceuticals Limited2025-10-17Human Prescription Drug Label7
RIVAROXABANAlembic Pharmaceuticals Inc. | Alembic Pharmaceuticals Limited2025-06-27Human Prescription Drug Label6