NDC 0069-7232

Caduet

Amlodipine And Atorvastatin

Caduet is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is Amlodipine Besylate; Atorvastatin Calcium Trihydrate.

• Product ID: 0069-7232_f6d65460-2cca-4fe6-a965-1d9b6c884665
• NDC: 0069-7232
• Product Type: Human Prescription Drug
• Proprietary Name: Caduet
• Generic Name: Amlodipine And Atorvastatin
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2022-08-31
• Marketing Category: NDA /
• Application Number: NDA021540
• Labeler Name: Pfizer Laboratories Div Pfizer Inc
• Substance Name: AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
• Active Ingredient Strength: 10 mg/1; mg/1
• Pharm Classes: Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0069-7232-30

30 TABLET, FILM COATED in 1 BOTTLE (0069-7232-30)

• Marketing Start Date: 2022-08-31
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Caduet" or generic name "Amlodipine And Atorvastatin"

NDC	Brand Name	Generic Name
0069-2150	Caduet	amlodipine besylate and atorvastatin calcium
0069-2160	Caduet	amlodipine besylate and atorvastatin calcium
0069-2170	Caduet	amlodipine besylate and atorvastatin calcium
0069-2180	Caduet	amlodipine besylate and atorvastatin calcium
0069-2190	Caduet	amlodipine besylate and atorvastatin calcium
0069-2260	Caduet	Caduet
0069-2250	Caduet	Caduet
0069-2960	Caduet	Caduet
0069-2270	Caduet	Caduet
0069-2970	Caduet	Caduet
0069-2980	Caduet	Caduet