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DIPYRIDAMOLE
DIPYRIDAMOLE - 64980-135-10 - (DIPYRIDAMOLE)
Drug Information of DIPYRIDAMOLE
| Product NDC: | 64980-135 |
| Proprietary Name: | DIPYRIDAMOLE |
| Non Proprietary Name: | DIPYRIDAMOLE |
| Active Ingredient(s): | 75 mg/1 & nbsp; DIPYRIDAMOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIPYRIDAMOLE
| Product NDC: | 64980-135 |
| Labeler Name: | Rising Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040733 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070213 |
Package Information of DIPYRIDAMOLE
| Package NDC: | 64980-135-10 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (64980-135-10) |
NDC Information of DIPYRIDAMOLE
| NDC Code | 64980-135-10 |
| Proprietary Name | DIPYRIDAMOLE |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (64980-135-10) |
| Product NDC | 64980-135 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIPYRIDAMOLE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070213 |
| Marketing Category Name | ANDA |
| Labeler Name | Rising Pharmaceuticals, Inc. |
| Substance Name | DIPYRIDAMOLE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC] |
