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Didanosine
Didanosine - 65862-313-50 - (Didanosine)
Drug Information of Didanosine
| Product NDC: | 65862-313 |
| Proprietary Name: | Didanosine |
| Non Proprietary Name: | Didanosine |
| Active Ingredient(s): | 400 mg/1 & nbsp; Didanosine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Didanosine
| Product NDC: | 65862-313 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090094 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080924 |
Package Information of Didanosine
| Package NDC: | 65862-313-50 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (65862-313-50) > 5 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of Didanosine
| NDC Code | 65862-313-50 |
| Proprietary Name | Didanosine |
| Package Description | 10 BLISTER PACK in 1 CARTON (65862-313-50) > 5 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 65862-313 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Didanosine |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080924 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | DIDANOSINE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |
