NDC 0024-1332

Plavix

Clopidogrel

Plavix is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Sanofi-aventis U.s. Llc. The primary component is Clopidogrel Bisulfate.

• Product ID: 0024-1332_4e097e4e-304d-4830-a350-d617662aa303
• NDC: 0024-1332
• Product Type: Human Prescription Drug
• Proprietary Name: Plavix
• Generic Name: Clopidogrel
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2009-05-09
• Marketing Category: NDA / NDA
• Application Number: NDA020839
• Labeler Name: sanofi-aventis U.S. LLC
• Substance Name: CLOPIDOGREL BISULFATE
• Active Ingredient Strength: 300 mg/1
• Pharm Classes: Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA],Cytochrome P450 2C8 Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 0024-1332-30

3 BLISTER PACK in 1 CARTON (0024-1332-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 2020-07-13
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Plavix" or generic name "Clopidogrel"

NDC	Brand Name	Generic Name
0024-1171	Plavix	clopidogrel
0024-1332	Plavix	clopidogrel
21695-665	Plavix	clopidogrel bisulfate
53808-0763	Plavix	Plavix
55289-911	Plavix	Plavix
63653-1332	Plavix	Plavix
63653-1171	Plavix	Plavix
67046-604	Plavix	Plavix
0093-7314	Clopidogrel	Clopidogrel
0615-7719	Clopidogrel	Clopidogrel
16714-052	Clopidogrel	Clopidogrel
16729-218	Clopidogrel	Clopidogrel
16729-219	Clopidogrel	Clopidogrel
31722-901	clopidogrel	clopidogrel
31722-902	clopidogrel	clopidogrel
33342-060	Clopidogrel	Clopidogrel
42543-713	Clopidogrel	clopidogrel
42543-714	Clopidogrel	clopidogrel
43547-484	CLOPIDOGREL	clopidogrel
43547-485	CLOPIDOGREL	clopidogrel
50090-4918	Clopidogrel	Clopidogrel
50090-5781	Clopidogrel	Clopidogrel
52605-082	clopidogrel	clopidogrel
0378-3627	Clopidogrel Bisulfate	clopidogrel
51079-558	Clopidogrel Bisulfate	clopidogrel