Product NDC: | 55154-8264 |
Proprietary Name: | Ketorolac Tromethamine |
Non Proprietary Name: | Ketorolac Tromethamine |
Active Ingredient(s): | 10 mg/1 & nbsp; Ketorolac Tromethamine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-8264 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074754 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100420 |
Package NDC: | 55154-8264-4 |
Package Description: | 100 POUCH in 1 CARTON (55154-8264-4) > 1 TABLET, FILM COATED in 1 POUCH (55154-8264-6) |
NDC Code | 55154-8264-4 |
Proprietary Name | Ketorolac Tromethamine |
Package Description | 100 POUCH in 1 CARTON (55154-8264-4) > 1 TABLET, FILM COATED in 1 POUCH (55154-8264-6) |
Product NDC | 55154-8264 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ketorolac Tromethamine |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100420 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | KETOROLAC TROMETHAMINE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |