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Didanosine
Didanosine - 65862-109-02 - (Didanosine)
Drug Information of Didanosine
| Product NDC: | 65862-109 |
| Proprietary Name: | Didanosine |
| Non Proprietary Name: | Didanosine |
| Active Ingredient(s): | 10 mg/mL & nbsp; Didanosine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Didanosine
| Product NDC: | 65862-109 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078112 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070308 |
Package Information of Didanosine
| Package NDC: | 65862-109-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (65862-109-02) > 200 mL in 1 BOTTLE |
NDC Information of Didanosine
| NDC Code | 65862-109-02 |
| Proprietary Name | Didanosine |
| Package Description | 1 BOTTLE in 1 CARTON (65862-109-02) > 200 mL in 1 BOTTLE |
| Product NDC | 65862-109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Didanosine |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20070308 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | DIDANOSINE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
