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Ocudox
Ocudox - 54799-535-60 - (Doxycycline Hyclate)
Drug Information of Ocudox
| Product NDC: | 54799-535 |
| Proprietary Name: | Ocudox |
| Non Proprietary Name: | Doxycycline Hyclate |
| Active Ingredient(s): | 50 mg/1 & nbsp; Doxycycline Hyclate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ocudox
| Product NDC: | 54799-535 |
| Labeler Name: | OCuSOFT INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062675 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110401 |
Package Information of Ocudox
| Package NDC: | 54799-535-60 |
| Package Description: | 60 CAPSULE in 1 BOTTLE (54799-535-60) |
NDC Information of Ocudox
| NDC Code | 54799-535-60 |
| Proprietary Name | Ocudox |
| Package Description | 60 CAPSULE in 1 BOTTLE (54799-535-60) |
| Product NDC | 54799-535 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Doxycycline Hyclate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | ANDA |
| Labeler Name | OCuSOFT INC. |
| Substance Name | DOXYCYCLINE HYCLATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
