Product NDC: | 62584-693 |
Proprietary Name: | Doxycycline |
Non Proprietary Name: | Doxycycline hyclate |
Active Ingredient(s): | 100 mg/1 & nbsp; Doxycycline hyclate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62584-693 |
Labeler Name: | American Health Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065095 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120301 |
Package NDC: | 62584-693-01 |
Package Description: | 10 BLISTER PACK in 1 CARTON (62584-693-01) > 10 TABLET, COATED in 1 BLISTER PACK (62584-693-11) |
NDC Code | 62584-693-01 |
Proprietary Name | Doxycycline |
Package Description | 10 BLISTER PACK in 1 CARTON (62584-693-01) > 10 TABLET, COATED in 1 BLISTER PACK (62584-693-11) |
Product NDC | 62584-693 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Doxycycline hyclate |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20120301 |
Marketing Category Name | ANDA |
Labeler Name | American Health Packaging |
Substance Name | DOXYCYCLINE HYCLATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes |