Details for New Drug Application (NDA): 211012
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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-seven suppliers are listed for this compound. Additional details are available on the doxycycline hyclate profile page.
Summary for 211012
| Tradename: | DOXYCYCLINE HYCLATE |
| Applicant: | Ajanta Pharma Ltd |
| Ingredient: | doxycycline hyclate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 211012
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DOXYCYCLINE HYCLATE | doxycycline hyclate | CAPSULE;ORAL | 211012 | ANDA | Ajanta Pharma USA Inc. | 27241-140 | 27241-140-42 | 50 CAPSULE in 1 BOTTLE (27241-140-42) |
| DOXYCYCLINE HYCLATE | doxycycline hyclate | CAPSULE;ORAL | 211012 | ANDA | Ajanta Pharma USA Inc. | 27241-141 | 27241-141-08 | 500 CAPSULE in 1 BOTTLE (27241-141-08) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | EQ 50MG BASE | ||||
| Approval Date: | Sep 24, 2018 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | CAPSULE;ORAL | Strength | EQ 100MG BASE | ||||
| Approval Date: | Sep 24, 2018 | TE: | RLD: | No | |||||
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