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
  • 62135-842 Sulfadiazine 500 mg Oral Tablet by Chartwell Rx, LLC

NDC QR Code

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NDC 52125-226 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.