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Quinine Sulfate
Quinine Sulfate - 53489-700-07 - (Quinine Sulfate)
Drug Information of Quinine Sulfate
| Product NDC: | 53489-700 |
| 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: | 53489-700 |
| Labeler Name: | Mutual Pharmaceutical Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021799 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20120723 |
Package Information of Quinine Sulfate
| Package NDC: | 53489-700-07 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (53489-700-07) |
NDC Information of Quinine Sulfate
| NDC Code | 53489-700-07 |
| Proprietary Name | Quinine Sulfate |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (53489-700-07) |
| Product NDC | 53489-700 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Quinine Sulfate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120723 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Mutual Pharmaceutical Company, Inc. |
| Substance Name | QUININE SULFATE |
| Strength Number | 324 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimalarial [EPC] |
