52125-226 : Sulfadiazine 500 mg Oral Tablet
| NDC: | 52125-226 |
| Labeler: | Remedyrepack Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Sulfadiazine |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA040091 |
| Rev. Date: |
Appearance:
| Markings: | E757 |
| Shapes: |
Capsule |
| Colors: |
 White |
| Size (mm): | 17 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 52125-226-02: 30 TABLET IN 1 BLISTER PACK (52125‑226‑02)
Active Ingredients:
- Sulfadiazine
Dosage Strength:
- 500 mg
Inactive Ingredients:
- Croscarmellose Sodium
- Docusate Sodium
- Cellulose, Microcrystalline
- Povidone K12
- Sodium Benzoate
- Sodium Starch Glycolate Type a Potato
- Stearic Acid
Pharmaceutical Classes:
- Sulfonamide Antibacterial [EPC]
- Sulfonamides [Chemical/Ingredient]
Related Products:
Based on records with the same trade name.- 0185-0757 Sulfadiazine 500 mg Oral Tablet by Eon Labs, Inc.
- 42806-757 Sulfadiazine 500 mg Oral Tablet by Epic Pharma, LLC
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.