Home
>
National Drug Code (NDC)
>
CEPHALEXIN
CEPHALEXIN - 16590-049-36 - (CEPHALEXIN)
Drug Information of CEPHALEXIN
| Product NDC: | 16590-049 |
| Proprietary Name: | CEPHALEXIN |
| Non Proprietary Name: | CEPHALEXIN |
| Active Ingredient(s): | 250 mg/5mL & nbsp; CEPHALEXIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEPHALEXIN
| Product NDC: | 16590-049 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065326 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071204 |
Package Information of CEPHALEXIN
| Package NDC: | 16590-049-36 |
| Package Description: | 200 mL in 1 BOTTLE (16590-049-36) |
NDC Information of CEPHALEXIN
| NDC Code | 16590-049-36 |
| Proprietary Name | CEPHALEXIN |
| Package Description | 200 mL in 1 BOTTLE (16590-049-36) |
| Product NDC | 16590-049 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEPHALEXIN |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20071204 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | CEPHALEXIN |
| Strength Number | 250 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
