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SUPRAX
SUPRAX - 54569-2861-2 - (cefixime)
Drug Information of SUPRAX
| Product NDC: | 54569-2861 |
| Proprietary Name: | SUPRAX |
| Non Proprietary Name: | cefixime |
| Active Ingredient(s): | 400 mg/1 & nbsp; cefixime |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUPRAX
| Product NDC: | 54569-2861 |
| Labeler Name: | A-S Medication Solutions LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065130 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080401 |
Package Information of SUPRAX
| Package NDC: | 54569-2861-2 |
| Package Description: | 1 TABLET in 1 BOTTLE (54569-2861-2) |
NDC Information of SUPRAX
| NDC Code | 54569-2861-2 |
| Proprietary Name | SUPRAX |
| Package Description | 1 TABLET in 1 BOTTLE (54569-2861-2) |
| Product NDC | 54569-2861 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cefixime |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080401 |
| Marketing Category Name | ANDA |
| Labeler Name | A-S Medication Solutions LLC |
| Substance Name | CEFIXIME |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
