65862-110 : Didanosine 10 mg/ml Oral Powder, for Solution
| NDC: | 65862-110 |
| Labeler: | Aurobindo Pharma Limited |
| Product Type: | Human Prescription Drug |
| Drug Name: | Didanosine |
| Dosage Form: | Oral Powder, for Solution |
| Application #: | ANDA078112 |
| Rev. Date: |
NDC Package Codes:
- 65862-110-04: 1 BOTTLE IN 1 CARTON (65862‑110‑04) > 400 ML IN 1 BOTTLE
Active Ingredients:
- Didanosine
Dosage Strength:
- 10 mg/mL
Pharmaceutical Classes:
- Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
- Nucleoside Analog [Chemical/Ingredient]
- Nucleoside Reverse Transcriptase Inhibitors [MoA]
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- More related products ...
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Related Discussions:
didanosineEC
What are side effects? ## Didanosine may cause tingling, burning or numbness in the hands and feet (peripheral neuropath... 2 replies
What are side effects? ## Didanosine may cause tingling, burning or numbness in the hands and feet (peripheral neuropath... 2 replies
Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
