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KETOROLAC TROMETHAMINE - 49349-753-01 - (KETOROLAC TROMETHAMINE)

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Drug Information of KETOROLAC TROMETHAMINE

Product NDC: 49349-753
Proprietary Name: KETOROLAC TROMETHAMINE
Non Proprietary Name: KETOROLAC TROMETHAMINE
Active Ingredient(s): 30    mg/mL & nbsp;   KETOROLAC TROMETHAMINE
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of KETOROLAC TROMETHAMINE

Product NDC: 49349-753
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077942
Marketing Category: ANDA
Start Marketing Date: 20130612

Package Information of KETOROLAC TROMETHAMINE

Package NDC: 49349-753-01
Package Description: 1 mL in 1 VIAL (49349-753-01)

NDC Information of KETOROLAC TROMETHAMINE

NDC Code 49349-753-01
Proprietary Name KETOROLAC TROMETHAMINE
Package Description 1 mL in 1 VIAL (49349-753-01)
Product NDC 49349-753
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name KETOROLAC TROMETHAMINE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR
Start Marketing Date 20130612
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name KETOROLAC TROMETHAMINE
Strength Number 30
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of KETOROLAC TROMETHAMINE


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