Details for New Drug Application (NDA): 062396
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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-four suppliers are listed for this compound. Additional details are available on the doxycycline hyclate profile page.
Summary for 062396
Tradename: | DOXYCYCLINE HYCLATE |
Applicant: | Hikma Intl Pharms |
Ingredient: | doxycycline hyclate |
Patents: | 0 |
Suppliers and Packaging for NDA: 062396
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DOXYCYCLINE HYCLATE | doxycycline hyclate | CAPSULE;ORAL | 062396 | ANDA | Hikma Pharmaceuticals USA Inc. | 0143-3141 | 0143-3141-50 | 50 CAPSULE, GELATIN COATED in 1 BOTTLE (0143-3141-50) |
DOXYCYCLINE HYCLATE | doxycycline hyclate | CAPSULE;ORAL | 062396 | ANDA | Hikma Pharmaceuticals USA Inc. | 0143-3142 | 0143-3142-05 | 500 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (0143-3142-05) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 100MG BASE | ||||
Approval Date: | May 7, 1984 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | EQ 50MG BASE | ||||
Approval Date: | Nov 7, 1984 | TE: | AB | RLD: | No |
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