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Milrinone Lactate - 0143-9709-10 - (Milrinone Lactate)

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Drug Information of Milrinone Lactate

Product NDC: 0143-9709
Proprietary Name: Milrinone Lactate
Non Proprietary Name: Milrinone Lactate
Active Ingredient(s): 20    mg/20mL & nbsp;   Milrinone Lactate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Milrinone Lactate

Product NDC: 0143-9709
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077966
Marketing Category: ANDA
Start Marketing Date: 20101203

Package Information of Milrinone Lactate

Package NDC: 0143-9709-10
Package Description: 20 mL in 1 VIAL (0143-9709-10)

NDC Information of Milrinone Lactate

NDC Code 0143-9709-10
Proprietary Name Milrinone Lactate
Package Description 20 mL in 1 VIAL (0143-9709-10)
Product NDC 0143-9709
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Milrinone Lactate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20101203
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name MILRINONE LACTATE
Strength Number 20
Strength Unit mg/20mL
Pharmaceutical Classes Phosphodiesterase 3 Inhibitor [EPC],Phosphodiesterase 3 Inhibitors [MoA]

Complete Information of Milrinone Lactate


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