0007-5180 : Altabax 10 mg/g Topical Ointment


NDC: 0007-5180
Labeler: Glaxosmithkline LLC
Product Type: Human Prescription Drug
Drug Name:  Altabax
Dosage Form: Topical Ointment
Application #: NDA022055
Rev. Date: 


NDC Package Codes:

  • 0007-5180-22: 15 G IN 1 TUBE (0007‑5180‑22)
  • 0007-5180-25: 1 TUBE IN 1 CARTON (0007‑5180‑25) > 30 G IN 1 TUBE
  • 0007-5180-64: 5 G IN 1 TUBE (0007‑5180‑64)

Active Ingredients:

  • Retapamulin

Dosage Strength:

  • 10 mg/g

Pharmaceutical Classes:

  • pleuromutilin [Chemical/Ingredient]
  • Pleuromutilin Antibacterial [EPC]

Related Products:

Based on records with the same trade name.
  • 16110-518 Altabax 10 mg Topical Ointment by Aqua Pharmaceuticals
  • 21695-644 Altabax 10 mg/g Topical Ointment by Rebel Distributors Corp.
  • 54868-6096 Altabax 10 mg/g Topical Ointment by Physicians Total Care, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 0007-5180 QR Code

< Prev: 0007-4896Next: 0008-0045 >




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.