| NDC Code | 0378-8886-05 |
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| Package Description | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0378-8886-05) |
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| Product NDC | 0378-8886 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Didanosine |
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| Non-Proprietary Name | Didanosine Enteric-coated Beadlets |
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| Dosage Form | CAPSULE, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20100628 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090788 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | DIDANOSINE |
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| Strength | 125 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
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