51672-5307 : Dapsone 75 mg/g Topical Gel


NDC51672-5307
Labeler: Taro Pharmaceuticals U.S.a., Inc.
Product Type: Human Prescription Drug
Drug Name:  Dapsone
Dosage Form: Topical Gel
Application #: NDA207154
Rev. Date: 


NDC Package Codes:

  • 51672-5307-3: 1 BOTTLE, PUMP IN 1 CARTON (51672‑5307‑3) > 60 G IN 1 BOTTLE, PUMP
  • 51672-5307-8: 1 BOTTLE, PUMP IN 1 CARTON (51672‑5307‑8) > 90 G IN 1 BOTTLE, PUMP

Active Ingredients:

  • Dapsone

Dosage Strength:

  • 75 mg/g

Pharmaceutical Classes:

  • Sulfone [EPC]
  • Sulfones [CS]

Related Products:

Based on records with the same trade name.
  • 51672-1387 Dapsone 50 mg/g Topical Gel by Taro Pharmaceuticals U.S.a., Inc.
  • 51672-1388 Dapsone 75 mg/g Topical Gel by Taro Pharmaceuticals U.S.a., Inc.
  • 51672-4197 Dapsone 25 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
  • 51672-4198 Dapsone 100 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
  • 0378-4830 Dapsone 75 mg/g Topical Gel by Mylan Pharmaceuticals Inc.
  • 0713-0886 Dapsone 50 mg/g Topical Gel by Cosette Pharmaceuticals, Inc.
  • 0904-7018 Dapsone 100 mg Oral Tablet by Major Pharmaceuticals
  • 0904-7019 Dapsone 25 mg Oral Tablet by Major Pharmaceuticals
  • 10135-654 Dapsone 25 mg Oral Tablet by Marlex Pharmaceuticals Inc
  • 10135-655 Dapsone 100 mg Oral Tablet by Marlex Pharmaceuticals Inc
  • 13668-605 Dapsone 75 mg/g Topical Gel by Torrent Pharmaceuticals Limited
  • 13925-504 Dapsone 25 mg Oral Tablet by Seton Pharmaceuticals
  • 13925-505 Dapsone 100 mg Oral Tablet by Seton Pharmaceuticals
  • 16714-956 Dapsone 50 mg/g Topical Gel by Northstar Rx LLC
  • 16714-975 Dapsone 75 mg/g Topical Gel by Northstar Rx LLC
  • 21922-018 Dapsone 50 mg/g Topical Gel by Encube Ethicals Private Limited
  • 29033-036 Dapsone 25 mg Oral Tablet by Nostrum Laboratories, Inc.
  • 29033-037 Dapsone 100 mg Oral Tablet by Nostrum Laboratories, Inc.
  • 42291-298 Dapsone 25 mg Oral Tablet by Avkare, Inc.
  • 42291-299 Dapsone 100 mg Oral Tablet by Avkare, Inc.
  • More related products ...

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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.