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AMOXICILLIN
AMOXICILLIN - 16590-647-30 - (AMOXICILLIN)
Drug Information of AMOXICILLIN
| Product NDC: | 16590-647 |
| Proprietary Name: | AMOXICILLIN |
| Non Proprietary Name: | AMOXICILLIN |
| Active Ingredient(s): | 125 mg/1 & nbsp; AMOXICILLIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMOXICILLIN
| Product NDC: | 16590-647 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064013 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100128 |
Package Information of AMOXICILLIN
| Package NDC: | 16590-647-30 |
| Package Description: | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16590-647-30) |
NDC Information of AMOXICILLIN
| NDC Code | 16590-647-30 |
| Proprietary Name | AMOXICILLIN |
| Package Description | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16590-647-30) |
| Product NDC | 16590-647 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMOXICILLIN |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20100128 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | AMOXICILLIN |
| Strength Number | 125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
