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SULFASALAZINE
SULFASALAZINE - 68788-9021-3 - (SULFASALAZINE)
Drug Information of SULFASALAZINE
| Product NDC: | 68788-9021 |
| Proprietary Name: | SULFASALAZINE |
| Non Proprietary Name: | SULFASALAZINE |
| Active Ingredient(s): | 500 mg/1 & nbsp; SULFASALAZINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SULFASALAZINE
| Product NDC: | 68788-9021 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087197 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100609 |
Package Information of SULFASALAZINE
| Package NDC: | 68788-9021-3 |
| Package Description: | 30 TABLET in 1 BOTTLE, DISPENSING (68788-9021-3) |
NDC Information of SULFASALAZINE
| NDC Code | 68788-9021-3 |
| Proprietary Name | SULFASALAZINE |
| Package Description | 30 TABLET in 1 BOTTLE, DISPENSING (68788-9021-3) |
| Product NDC | 68788-9021 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SULFASALAZINE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100609 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | SULFASALAZINE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient] |
