Sulfasalazine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.. The primary component is Sulfasalazine.
Product ID | 23155-019_16f2debd-460c-4a6e-a47d-a4520406ad54 |
NDC | 23155-019 |
Product Type | Human Prescription Drug |
Proprietary Name | Sulfasalazine |
Generic Name | Sulfasalazine |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 1973-11-12 |
Marketing Category | ANDA / |
Application Number | ANDA080197 |
Labeler Name | HERITAGE PHARMACEUTICALS INC. D/B/A AVET PHARMACEUTICALS INC. |
Substance Name | SULFASALAZINE |
Active Ingredient Strength | 500 mg/1 |
Pharm Classes | Aminosalicylate [EPC],Aminosalicylic Acids [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2021-05-07 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
0093-3234 | Sulfasalazine | Sulfasalazine |
0591-0796 | Sulfasalazine | Sulfasalazine |
0603-5801 | Sulfasalazine | sulfasalazine |
10544-288 | Sulfasalazine | sulfasalazine |
23155-019 | Sulfasalazine | Sulfasalazine |
33261-756 | Sulfasalazine | sulfasalazine |
43353-495 | Sulfasalazine | Sulfasalazine |
50090-0086 | Sulfasalazine | Sulfasalazine |
50090-2013 | Sulfasalazine | Sulfasalazine |
50268-730 | Sulfasalazine | Sulfasalazine |
59762-0104 | Sulfasalazine | Sulfasalazine |
68071-4215 | Sulfasalazine | Sulfasalazine |
68788-9021 | SULFASALAZINE | SULFASALAZINE |
70518-0185 | Sulfasalazine | Sulfasalazine |
70518-1829 | Sulfasalazine | Sulfasalazine |
59762-5000 | Sulfasalazine | Sulfasalazine |
63629-5688 | Sulfasalazine | Sulfasalazine |
70518-2342 | Sulfasalazine | Sulfasalazine |
0013-0101 | Azulfidine | Sulfasalazine |
0013-0102 | Azulfidine | Sulfasalazine |