21695-644 : Altabax 10 mg/g Topical Ointment


NDC: 21695-644
Labeler: Rebel Distributors Corp.
Product Type: Human Prescription Drug
Drug Name:  Altabax
Dosage Form: Topical Ointment
Application #: NDA022055
Rev. Date: 


NDC Package Codes:

  • 21695-644-10: 10 G IN 1 TUBE (21695‑644‑10)

Active Ingredients:

  • Retapamulin

Dosage Strength:

  • 10 mg/g

Pharmaceutical Classes:

  • Diterpenes [CS]
  • Pleuromutilin Antibacterial [EPC]

Related Products:

Based on records with the same trade name.
  • 0007-5180 Altabax 10 mg/g Topical Ointment by Glaxosmithkline LLC
  • 16110-518 Altabax 10 mg Topical Ointment by Aqua Pharmaceuticals
  • 54868-6096 Altabax 10 mg/g Topical Ointment by Physicians Total Care, Inc.

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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.