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AMOXICILLIN
AMOXICILLIN - 12634-183-81 - (AMOXICILLIN)
Drug Information of AMOXICILLIN
| Product NDC: | 12634-183 |
| Proprietary Name: | AMOXICILLIN |
| Non Proprietary Name: | AMOXICILLIN |
| Active Ingredient(s): | 250 mg/1 & nbsp; AMOXICILLIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMOXICILLIN
| Product NDC: | 12634-183 |
| Labeler Name: | Apotheca Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065271 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050308 |
Package Information of AMOXICILLIN
| Package NDC: | 12634-183-81 |
| Package Description: | 21 CAPSULE in 1 BOTTLE (12634-183-81) |
NDC Information of AMOXICILLIN
| NDC Code | 12634-183-81 |
| Proprietary Name | AMOXICILLIN |
| Package Description | 21 CAPSULE in 1 BOTTLE (12634-183-81) |
| Product NDC | 12634-183 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMOXICILLIN |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20050308 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotheca Inc. |
| Substance Name | AMOXICILLIN |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
