Details for New Drug Application (NDA): 212610
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The generic ingredient in DOXYCYCLINE HYCLATE is doxycycline hyclate. There are twenty-eight drug master file entries for this compound. Seventy-six suppliers are listed for this compound. Additional details are available on the doxycycline hyclate profile page.
Summary for 212610
| Tradename: | DOXYCYCLINE HYCLATE |
| Applicant: | Zhejiang Yongtai |
| Ingredient: | doxycycline hyclate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 212610
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DOXYCYCLINE HYCLATE | doxycycline hyclate | CAPSULE;ORAL | 212610 | ANDA | Zhejiang Yongtai Pharmaceutical Co., Ltd | 69434-016 | 69434-016-03 | 500 CAPSULE in 1 BOTTLE (69434-016-03) |
| DOXYCYCLINE HYCLATE | doxycycline hyclate | CAPSULE;ORAL | 212610 | ANDA | Zhejiang Yongtai Pharmaceutical Co., Ltd | 69434-016 | 69434-016-06 | 50 CAPSULE in 1 BOTTLE (69434-016-06) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | EQ 50MG BASE | ||||
| Approval Date: | Mar 31, 2020 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | EQ 100MG BASE | ||||
| Approval Date: | Mar 31, 2020 | TE: | RLD: | No | |||||
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