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Cephalexin
Cephalexin - 61442-202-01 - (Cephalexin)
Drug Information of Cephalexin
| Product NDC: | 61442-202 |
| Proprietary Name: | Cephalexin |
| Non Proprietary Name: | Cephalexin |
| Active Ingredient(s): | 250 mg/5mL & nbsp; Cephalexin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cephalexin
| Product NDC: | 61442-202 |
| Labeler Name: | Carlsbad Technology, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065336 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090601 |
Package Information of Cephalexin
| Package NDC: | 61442-202-01 |
| Package Description: | 24 BOTTLE in 1 BOX (61442-202-01) > 100 mL in 1 BOTTLE |
NDC Information of Cephalexin
| NDC Code | 61442-202-01 |
| Proprietary Name | Cephalexin |
| Package Description | 24 BOTTLE in 1 BOX (61442-202-01) > 100 mL in 1 BOTTLE |
| Product NDC | 61442-202 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cephalexin |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | ANDA |
| Labeler Name | Carlsbad Technology, Inc. |
| Substance Name | CEPHALEXIN |
| Strength Number | 250 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
