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Amoxicillin
Amoxicillin - 21695-385-00 - (Amoxicillin)
Drug Information of Amoxicillin
| Product NDC: | 21695-385 |
| Proprietary Name: | Amoxicillin |
| Non Proprietary Name: | Amoxicillin |
| Active Ingredient(s): | 250 mg/5mL & nbsp; Amoxicillin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amoxicillin
| Product NDC: | 21695-385 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA061931 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100201 |
Package Information of Amoxicillin
| Package NDC: | 21695-385-00 |
| Package Description: | 100 mL in 1 BOTTLE (21695-385-00) |
NDC Information of Amoxicillin
| NDC Code | 21695-385-00 |
| Proprietary Name | Amoxicillin |
| Package Description | 100 mL in 1 BOTTLE (21695-385-00) |
| Product NDC | 21695-385 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amoxicillin |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | AMOXICILLIN |
| Strength Number | 250 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
