NDC Code |
53808-0236-1 |
Proprietary Name |
Didanosine |
Package Description |
30 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (53808-0236-1) |
Product NDC |
53808-0236 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Didanosine |
Dosage Form Name |
CAPSULE, DELAYED RELEASE PELLETS |
Route Name |
ORAL |
Start Marketing Date |
20090701 |
Marketing Category Name |
ANDA |
Labeler Name |
State of Florida DOH Central Pharmacy |
Substance Name |
DIDANOSINE |
Strength Number |
250 |
Strength Unit |
mg/1 |
Pharmaceutical Classes |
Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA] |