21922-020 : Tavaborole 43.5 mg/ml Topical Solution


NDC: 21922-020
Labeler: Encube Ethicals Private Limited
Product Type: Human Prescription Drug
Drug Name:  Tavaborole
Dosage Form: Topical Solution
Application #: ANDA211297
Rev. Date: 


NDC Package Codes:

  • 21922-020-12: 1 BOTTLE, WITH APPLICATOR IN 1 CARTON (21922‑020‑12) > 10 ML IN 1 BOTTLE, WITH APPLICATOR

Active Ingredients:

  • Tavaborole

Dosage Strength:

  • 43.5 mg/mL

Pharmaceutical Classes:

  • Oxaborole Antifungal [EPC]
  • Protein Synthesis Inhibitors [MoA]
  • Boron Compounds [CS]

Related Products:

Based on records with the same trade name.
  • 0574-0157 Tavaborole 43.5 mg/ml Topical Solution by Paddock Laboratories, LLC.
  • 51672-1397 Tavaborole 43.5 mg/ml Topical Solution by Taro Pharmaceuticals U.S.a., Inc.
  • 51862-690 Tavaborole 43.5 mg/ml Topical Solution by Mayne Pharma Inc.
  • 62135-663 Tavaborole 43.5 mg/ml Topical Solution by Chartwell Rx, LLC
  • 62332-467 Tavaborole 43.5 mg/ml Topical Solution by Alembic Pharmaceuticals, Inc.
  • 63629-8704 Tavaborole 43.5 mg/ml Topical Solution by Bryant Ranch Prepack
  • 68180-958 Tavaborole 43.5 mg/ml Topical Solution by Lupin Pharmaceuticals, Inc.
  • 69097-686 Tavaborole 43.5 mg/ml Topical Solution by Cipla USA Inc.
  • 69238-1657 Tavaborole 43.5 mg/ml Topical Solution by Amneal Pharmaceuticals Ny LLC
  • 70771-1826 Tavaborole 43.5 mg/ml Topical Solution by Zydus Lifesciences Limited
  • 72578-102 Tavaborole 43.5 mg/ml Topical Solution by Viona Pharmaceuticals Inc

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