Details for New Drug Application (NDA): 091605
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The generic ingredient in DOXYCYCLINE 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 091605
| Tradename: | DOXYCYCLINE |
| Applicant: | Heritage |
| Ingredient: | doxycycline |
| Patents: | 0 |
Suppliers and Packaging for NDA: 091605
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DOXYCYCLINE | doxycycline | TABLET;ORAL | 091605 | ANDA | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-133 | 23155-133-01 | 100 TABLET in 1 BOTTLE (23155-133-01) |
| DOXYCYCLINE | doxycycline | TABLET;ORAL | 091605 | ANDA | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-133 | 23155-133-05 | 500 TABLET in 1 BOTTLE (23155-133-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 50MG BASE | ||||
| Approval Date: | Dec 20, 2011 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 75MG BASE | ||||
| Approval Date: | Dec 20, 2011 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 100MG BASE | ||||
| Approval Date: | Dec 20, 2011 | TE: | AB | RLD: | No | ||||
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