 
                        | Product NDC: | 54868-2391 | 
| Proprietary Name: | Minocycline hydrochloride | 
| Non Proprietary Name: | Minocycline hydrochloride | 
| Active Ingredient(s): | 100 mg/1 & nbsp; Minocycline hydrochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | CAPSULE | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 54868-2391 | 
| Labeler Name: | Physicians Total Care, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA065062 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 19930930 | 
| Package NDC: | 54868-2391-6 | 
| Package Description: | 20 CAPSULE in 1 BOTTLE (54868-2391-6) | 
| NDC Code | 54868-2391-6 | 
| Proprietary Name | Minocycline hydrochloride | 
| Package Description | 20 CAPSULE in 1 BOTTLE (54868-2391-6) | 
| Product NDC | 54868-2391 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Minocycline hydrochloride | 
| Dosage Form Name | CAPSULE | 
| Route Name | ORAL | 
| Start Marketing Date | 19930930 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Physicians Total Care, Inc. | 
| Substance Name | MINOCYCLINE HYDROCHLORIDE | 
| Strength Number | 100 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |