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Ketorolac Tromethamine
Ketorolac Tromethamine - 68387-440-20 - (Ketorolac Tromethamine)
Drug Information of Ketorolac Tromethamine
| Product NDC: | 68387-440 |
| 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) |
Labeler Information of Ketorolac Tromethamine
| Product NDC: | 68387-440 |
| Labeler Name: | Keltman Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074754 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100420 |
Package Information of Ketorolac Tromethamine
| Package NDC: | 68387-440-20 |
| Package Description: | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-440-20) |
NDC Information of Ketorolac Tromethamine
| NDC Code | 68387-440-20 |
| Proprietary Name | Ketorolac Tromethamine |
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-440-20) |
| Product NDC | 68387-440 |
| 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 | Keltman Pharmaceuticals Inc. |
| Substance Name | KETOROLAC TROMETHAMINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
