CLOPIDOGREL

Product NDC
67877-276
11-digit product format
678770276
Labeler code
67877
Product ID
67877-276_04c45152-3a50-45e1-9edb-2ddf3ed43988
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CLOPIDOGREL BISULFATE
Dosage form
TABLET
Route
ORAL
Labeler
Ascend Laboratories, LLC
Application
ANDA203632
Marketing category
ANDA
Marketing start
2024-05-16
Substance
CLOPIDOGREL BISULFATE
Active strength
75 mg/1
Pharmacologic classes
Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
08I79HTP27CLOPIDOGREL BISULFATE120202-66-6CLOPIDOGREL BISULFATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
67877-276-0567877027605500 TABLET in 1 BOTTLE (67877-276-05) 500 tablet2024-05-16NoNoHistorical
67877-276-306787702763030 TABLET in 1 BOTTLE (67877-276-30) 30 tablet2024-05-16NoNoHistorical
67877-276-906787702769090 TABLET in 1 BOTTLE (67877-276-90) 90 tablet2024-05-16NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CLOPIDOGRELREMEDYREPACK INC.2025-06-27HUMAN PRESCRIPTION DRUG LABEL1
CLOPIDOGRELA-S Medication Solutions2024-12-06Human Prescription Drug Label1
CLOPIDOGRELA-S Medication Solutions2024-12-06Human Prescription Drug Label1
CLOPIDOGRELAscend Laboratories, LLC | Alkem Laboratories Limited2024-05-15Human Prescription Drug Label8