61786-810 : Mupirocin 20 mg/g Topical Ointment
NDC: | 61786-810 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Mupirocin |
Dosage Form: | Topical Ointment |
Application #: | ANDA090480 |
Rev. Date: |
NDC Package Codes:
- 61786-810-47: 22 G IN 1 TUBE (61786‑810‑47)
Active Ingredients:
- Mupirocin
Dosage Strength:
- 20 mg/g
Pharmaceutical Classes:
- RNA Synthetase Inhibitor Antibacterial [EPC]
- RNA Synthetase Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 61786-473 Mupirocin 2 g/100g Topical Cream by Remedyrepack Inc.
- 52125-239 Mupirocin 20 mg/g Topical Ointment by Remedyrepack Inc.
- 52125-545 Mupirocin 20 mg/g Topical Ointment by Remedyrepack Inc.
- 70518-0292 Mupirocin 20 mg/g Topical Ointment by Remedyrepack Inc.
- 70518-1808 Mupirocin 20 mg/g Topical Ointment by Remedyrepack Inc.
- 70518-2344 Mupirocin 20 mg/g Topical Ointment by Remedyrepack Inc.
- 70518-3774 Mupirocin 20 mg/g Topical Cream by Remedyrepack Inc.
- 0093-1010 Mupirocin 20 mg/g Topical Ointment by Teva Pharmaceuticals USA Inc
- 0168-0352 Mupirocin 20 mg/g Topical Ointment by E. Fougera & Co., a Division of Fougera Pharmaceuticals Inc.
- 0904-7284 Mupirocin 20 mg/g Topical Ointment by Major Pharmaceuticals
- 16590-158 Mupirocin 20 mg/g Topical Ointment by Stat Rx LLC USA
- 16714-055 Mupirocin 20 mg/g Topical Cream by Northstar Rx LLC
- 17856-0112 Mupirocin 20 mg/g Topical Ointment by Atlantic Biologicals Corps
- 21695-188 Mupirocin 20 mg/g Topical Ointment by Rebel Distributors Corp.
- 21922-029 Mupirocin 2 g/100g Topical Cream by Encube Ethicals Private Limited
- 42254-137 Mupirocin 20 mg/g Topical Ointment by Rebel Distributors Corp
- 42254-229 Mupirocin 20 mg/g Topical Ointment by Rebel Distributors Corp
- 45802-018 Mupirocin 20 mg/g Topical Cream by Padagis Israel Pharmaceuticals Ltd
- 45802-112 Mupirocin 20 mg/g Topical Ointment by Perrigo New York Inc
- 45865-722 Mupirocin 20 mg/g Topical Ointment by Medsource Pharmaceuticals
- 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.