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Clindamycin - 63323-282-04 - (CLINDAMYCIN PHOSPHATE)

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Drug Information of Clindamycin

Product NDC: 63323-282
Proprietary Name: Clindamycin
Non Proprietary Name: CLINDAMYCIN PHOSPHATE
Active Ingredient(s): 150    mg/mL & nbsp;   CLINDAMYCIN PHOSPHATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Clindamycin

Product NDC: 63323-282
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065347
Marketing Category: ANDA
Start Marketing Date: 20091122

Package Information of Clindamycin

Package NDC: 63323-282-04
Package Description: 25 VIAL in 1 TRAY (63323-282-04) > 4 mL in 1 VIAL

NDC Information of Clindamycin

NDC Code 63323-282-04
Proprietary Name Clindamycin
Package Description 25 VIAL in 1 TRAY (63323-282-04) > 4 mL in 1 VIAL
Product NDC 63323-282
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CLINDAMYCIN PHOSPHATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20091122
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name CLINDAMYCIN PHOSPHATE
Strength Number 150
Strength Unit mg/mL
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of Clindamycin


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