Home
>
National Drug Code (NDC)
>
Biaxin
Biaxin - 0074-3165-41 - (Clarithromycin)
Drug Information of Biaxin
| Product NDC: | 0074-3165 |
| 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, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Biaxin
| Product NDC: | 0074-3165 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050775 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000303 |
Package Information of Biaxin
| Package NDC: | 0074-3165-41 |
| Package Description: | 4 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-3165-41) > 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Biaxin
| NDC Code | 0074-3165-41 |
| Proprietary Name | Biaxin |
| Package Description | 4 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-3165-41) > 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 0074-3165 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clarithromycin |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20000303 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| Substance Name | CLARITHROMYCIN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
