NDC 70882-123

Clopidogrel Kit

Clopidogrel Kit

Clopidogrel Kit is a Kit in the Human Prescription Drug category. It is labeled and distributed by Cambridge Therapeutics Technologies, Llc. The primary component is .

• Product ID: 70882-123_126c5279-0ac1-4ed8-8c0f-b9084e3d7bb2
• NDC: 70882-123
• Product Type: Human Prescription Drug
• Proprietary Name: Clopidogrel Kit
• Generic Name: Clopidogrel Kit
• Dosage Form: Kit
• Marketing Start Date: 2017-07-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA076274
• Labeler Name: Cambridge Therapeutics Technologies, LLC
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 70882-123-01

1 KIT in 1 KIT (70882-123-01) * 30 TABLET, COATED in 1 BLISTER PACK (70882-122-30) * 30 TABLET, FILM COATED in 1 BLISTER PACK (70882-116-30)

• Marketing Start Date: 2017-07-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70882-123-01 [70882012301]

Clopidogrel Kit KIT

• Marketing Category: ANDA
• Application Number: ANDA076274
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-07-01
• Inactivation Date: 2020-01-31

Drug Details

OpenFDA Data

• SPL SET ID: 126c5279-0ac1-4ed8-8c0f-b9084e3d7bb2
• Manufacturer:
  • Cambridge Therapeutics Technologies, LLC
• RxNorm Concept Unique ID - RxCUI:
  • 308416
  • 309362