Details for New Drug Application (NDA): 209582
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The generic ingredient in DOXYCYCLINE is doxycycline hyclate. There are twenty-eight drug master file entries for this compound. Seventy-four suppliers are listed for this compound. Additional details are available on the doxycycline hyclate profile page.
Summary for 209582
Tradename: | DOXYCYCLINE |
Applicant: | Zydus Pharms |
Ingredient: | doxycycline |
Patents: | 0 |
Suppliers and Packaging for NDA: 209582
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DOXYCYCLINE | doxycycline | TABLET;ORAL | 209582 | ANDA | A-S Medication Solutions | 50090-3809 | 50090-3809-0 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-3809-0) |
DOXYCYCLINE | doxycycline | TABLET;ORAL | 209582 | ANDA | Zydus Pharmaceuticals USA Inc. | 70710-1121 | 70710-1121-1 | 100 TABLET, FILM COATED in 1 BOTTLE (70710-1121-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 50MG BASE | ||||
Approval Date: | Sep 28, 2017 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 75MG BASE | ||||
Approval Date: | Sep 28, 2017 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 100MG BASE | ||||
Approval Date: | Sep 28, 2017 | TE: | AB | RLD: | No |
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