| NDC Code | 0378-8887-05 |
|---|
| Package Description | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-8887-05) |
|---|
| Product NDC | 0378-8887 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Didanosine |
|---|
| Non-Proprietary Name | Didanosine Enteric-coated Beadlets |
|---|
| Dosage Form | CAPSULE, DELAYED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100628 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090788 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | DIDANOSINE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
|---|