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QUALAQUIN
QUALAQUIN - 16590-595-90 - (QUININE SULFATE)
Drug Information of QUALAQUIN
| Product NDC: | 16590-595 |
| Proprietary Name: | QUALAQUIN |
| Non Proprietary Name: | QUININE SULFATE |
| Active Ingredient(s): | 324 mg/1 & nbsp; QUININE SULFATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of QUALAQUIN
| Product NDC: | 16590-595 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021799 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050812 |
Package Information of QUALAQUIN
| Package NDC: | 16590-595-90 |
| Package Description: | 90 CAPSULE in 1 BOTTLE (16590-595-90) |
NDC Information of QUALAQUIN
| NDC Code | 16590-595-90 |
| Proprietary Name | QUALAQUIN |
| Package Description | 90 CAPSULE in 1 BOTTLE (16590-595-90) |
| Product NDC | 16590-595 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | QUININE SULFATE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20050812 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | QUININE SULFATE |
| Strength Number | 324 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimalarial [EPC] |
