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Moxatag
Moxatag - 59630-142-03 - (amoxicillin)
Drug Information of Moxatag
| Product NDC: | 59630-142 |
| Proprietary Name: | Moxatag |
| Non Proprietary Name: | amoxicillin |
| Active Ingredient(s): | 775 mg/1 & nbsp; amoxicillin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Moxatag
| Product NDC: | 59630-142 |
| Labeler Name: | Shionogi Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050813 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110826 |
Package Information of Moxatag
| Package NDC: | 59630-142-03 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59630-142-03) |
NDC Information of Moxatag
| NDC Code | 59630-142-03 |
| Proprietary Name | Moxatag |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59630-142-03) |
| Product NDC | 59630-142 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amoxicillin |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110826 |
| Marketing Category Name | NDA |
| Labeler Name | Shionogi Inc. |
| Substance Name | AMOXICILLIN |
| Strength Number | 775 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
