| NDC Code: |
68462-563 |
| Proprietary Name: |
Atovaquone and Proguanil Hydrochloride |
| Suffix: |
Pediatric |
| Non-Proprietary Name: |
atovaquone and proguanil hydrochloride |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
15-09-2011 |
| Category Name: |
NDA AUTHORIZED GENERIC |
| Application Number: |
NDA021078 |
| Labeler: |
GLENMARK GENERICS INC |
| Substance Name: |
ATOVAQUONE; PROGUANIL HYDROCHLORIDE |
| Active Numerator Strength: |
62.5; 25 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Antimalarial [EPC],Antiprotozoal [EPC],Antimalarial [EPC],Dihydrofolate Reductase Inhibitors [MoA] |
| DEA Schedule: |
|
