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DORYX
DORYX - 0430-0114-20 - (doxycycline hyclate)
Drug Information of DORYX
| Product NDC: | 0430-0114 |
| Proprietary Name: | DORYX |
| Non Proprietary Name: | doxycycline hyclate |
| Active Ingredient(s): | 200 mg/1 & nbsp; doxycycline hyclate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DORYX
| Product NDC: | 0430-0114 |
| Labeler Name: | Warner Chilcott (US), LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050795 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130701 |
Package Information of DORYX
| Package NDC: | 0430-0114-20 |
| Package Description: | 48 BOTTLE in 1 CASE (0430-0114-20) > 60 TABLET, DELAYED RELEASE in 1 BOTTLE |
NDC Information of DORYX
| NDC Code | 0430-0114-20 |
| Proprietary Name | DORYX |
| Package Description | 48 BOTTLE in 1 CASE (0430-0114-20) > 60 TABLET, DELAYED RELEASE in 1 BOTTLE |
| Product NDC | 0430-0114 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | doxycycline hyclate |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | NDA |
| Labeler Name | Warner Chilcott (US), LLC |
| Substance Name | DOXYCYCLINE HYCLATE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
