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Tranexamic Acid
Tranexamic Acid - 0591-3720-30 - (Tranexamic Acid)
Drug Information of Tranexamic Acid
| Product NDC: | 0591-3720 |
| Proprietary Name: | Tranexamic Acid |
| Non Proprietary Name: | Tranexamic Acid |
| Active Ingredient(s): | 650 mg/1 & nbsp; Tranexamic Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tranexamic Acid
| Product NDC: | 0591-3720 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202093 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130103 |
Package Information of Tranexamic Acid
| Package NDC: | 0591-3720-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3720-30) |
NDC Information of Tranexamic Acid
| NDC Code | 0591-3720-30 |
| Proprietary Name | Tranexamic Acid |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3720-30) |
| Product NDC | 0591-3720 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tranexamic Acid |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130103 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | TRANEXAMIC ACID |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE] |
