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Biaxin
Biaxin - 52125-103-02 - (Clarithromycin)
Drug Information of Biaxin
| Product NDC: | 52125-103 |
| Proprietary Name: | Biaxin |
| Non Proprietary Name: | Clarithromycin |
| Active Ingredient(s): | 500 mg/1 & nbsp; Clarithromycin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Biaxin
| Product NDC: | 52125-103 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050662 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130225 |
Package Information of Biaxin
| Package NDC: | 52125-103-02 |
| Package Description: | 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-103-02) |
NDC Information of Biaxin
| NDC Code | 52125-103-02 |
| Proprietary Name | Biaxin |
| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-103-02) |
| Product NDC | 52125-103 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clarithromycin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130225 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | CLARITHROMYCIN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
