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Quinine Sulfate
Quinine Sulfate - 0378-7180-01 - (quinine sulfate)
Drug Information of Quinine Sulfate
| Product NDC: | 0378-7180 |
| Proprietary Name: | Quinine Sulfate |
| 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 Quinine Sulfate
| Product NDC: | 0378-7180 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202581 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130506 |
Package Information of Quinine Sulfate
| Package NDC: | 0378-7180-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-7180-01) |
NDC Information of Quinine Sulfate
| NDC Code | 0378-7180-01 |
| Proprietary Name | Quinine Sulfate |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-7180-01) |
| Product NDC | 0378-7180 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | quinine sulfate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130506 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | QUININE SULFATE |
| Strength Number | 324 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimalarial [EPC] |
