Details for New Drug Application (NDA): 040150
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The generic ingredient in HYDROXYCHLOROQUINE SULFATE is hydroxychloroquine sulfate. There are fifteen drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the hydroxychloroquine sulfate profile page.
Summary for 040150
| Tradename: | HYDROXYCHLOROQUINE SULFATE |
| Applicant: | Creekwood Pharms |
| Ingredient: | hydroxychloroquine sulfate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 040150
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| HYDROXYCHLOROQUINE SULFATE | hydroxychloroquine sulfate | TABLET;ORAL | 040150 | ANDA | Bryant Ranch Prepack | 71335-2813 | 71335-2813-1 | 100 TABLET in 1 BOTTLE (71335-2813-1) |
| HYDROXYCHLOROQUINE SULFATE | hydroxychloroquine sulfate | TABLET;ORAL | 040150 | ANDA | Bryant Ranch Prepack | 71335-2814 | 71335-2814-1 | 500 TABLET in 1 BOTTLE (71335-2814-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
| Approval Date: | Jan 27, 1996 | TE: | AB | RLD: | No | ||||
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