Product NDC: | 11819-311 |
Proprietary Name: | Doxycycline Hyclate |
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: | 11819-311 |
Labeler Name: | HHS/Program Support Center/Supply Service Center |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065095 |
Marketing Category: | ANDA |
Start Marketing Date: | 20030702 |
Package NDC: | 11819-311-30 |
Package Description: | 30 TABLET, COATED in 1 BOTTLE (11819-311-30) |
NDC Code | 11819-311-30 |
Proprietary Name | Doxycycline Hyclate |
Package Description | 30 TABLET, COATED in 1 BOTTLE (11819-311-30) |
Product NDC | 11819-311 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Doxycycline hyclate |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20030702 |
Marketing Category Name | ANDA |
Labeler Name | HHS/Program Support Center/Supply Service Center |
Substance Name | DOXYCYCLINE HYCLATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes |