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CEPHALEXIN
CEPHALEXIN - 63304-959-02 - (CEPHALEXIN)
Drug Information of CEPHALEXIN
| Product NDC: | 63304-959 |
| 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: | 63304-959 |
| Labeler Name: | Ranbaxy Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065081 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20011029 |
Package Information of CEPHALEXIN
| Package NDC: | 63304-959-02 |
| Package Description: | 200 mL in 1 BOTTLE (63304-959-02) |
NDC Information of CEPHALEXIN
| NDC Code | 63304-959-02 |
| Proprietary Name | CEPHALEXIN |
| Package Description | 200 mL in 1 BOTTLE (63304-959-02) |
| Product NDC | 63304-959 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEPHALEXIN |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20011029 |
| Marketing Category Name | ANDA |
| Labeler Name | Ranbaxy Pharmaceuticals Inc. |
| Substance Name | CEPHALEXIN |
| Strength Number | 250 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
