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Sulfadiazine
Sulfadiazine - 0185-0757-10 - (Sulfadiazine)
Drug Information of Sulfadiazine
| Product NDC: | 0185-0757 |
| Proprietary Name: | Sulfadiazine |
| Non Proprietary Name: | Sulfadiazine |
| Active Ingredient(s): | 500 mg/1 & nbsp; Sulfadiazine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulfadiazine
| Product NDC: | 0185-0757 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040091 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19940729 |
Package Information of Sulfadiazine
| Package NDC: | 0185-0757-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0185-0757-10) |
NDC Information of Sulfadiazine
| NDC Code | 0185-0757-10 |
| Proprietary Name | Sulfadiazine |
| Package Description | 1000 TABLET in 1 BOTTLE (0185-0757-10) |
| Product NDC | 0185-0757 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sulfadiazine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19940729 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | SULFADIAZINE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
