Product NDC: | 24236-049 |
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): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24236-049 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062396 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120112 |
Package NDC: | 24236-049-60 |
Package Description: | 60 CAPSULE in 1 VIAL (24236-049-60) |
NDC Code | 24236-049-60 |
Proprietary Name | Doxycycline Hyclate |
Package Description | 60 CAPSULE in 1 VIAL (24236-049-60) |
Product NDC | 24236-049 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Doxycycline Hyclate |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20120112 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | DOXYCYCLINE HYCLATE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |