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Oracea
Oracea - 54868-5676-0 - (doxycycline)
Drug Information of Oracea
| Product NDC: | 54868-5676 |
| Proprietary Name: | Oracea |
| Non Proprietary Name: | doxycycline |
| Active Ingredient(s): | 40 mg/1 & nbsp; doxycycline |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE PELLETS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oracea
| Product NDC: | 54868-5676 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA050805 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060929 |
Package Information of Oracea
| Package NDC: | 54868-5676-0 |
| Package Description: | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (54868-5676-0) |
NDC Information of Oracea
| NDC Code | 54868-5676-0 |
| Proprietary Name | Oracea |
| Package Description | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (54868-5676-0) |
| Product NDC | 54868-5676 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | doxycycline |
| Dosage Form Name | CAPSULE, DELAYED RELEASE PELLETS |
| Route Name | ORAL |
| Start Marketing Date | 20060929 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DOXYCYCLINE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
