 
                        | Product NDC: | 0245-0144 | 
| Proprietary Name: | Pacerone | 
| Non Proprietary Name: | Amiodarone Hydrochloride | 
| Active Ingredient(s): | 100 mg/1 & nbsp; Amiodarone Hydrochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0245-0144 | 
| Labeler Name: | Upsher-Smith Laboratories, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA075135 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20110119 | 
| Package NDC: | 0245-0144-01 | 
| Package Description: | 10 BLISTER PACK in 1 CARTON (0245-0144-01) > 10 TABLET in 1 BLISTER PACK (0245-0144-89) | 
| NDC Code | 0245-0144-01 | 
| Proprietary Name | Pacerone | 
| Package Description | 10 BLISTER PACK in 1 CARTON (0245-0144-01) > 10 TABLET in 1 BLISTER PACK (0245-0144-89) | 
| Product NDC | 0245-0144 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Amiodarone Hydrochloride | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20110119 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Upsher-Smith Laboratories, Inc. | 
| Substance Name | AMIODARONE HYDROCHLORIDE | 
| Strength Number | 100 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Antiarrhythmic [EPC] |