Prescription drug · ANDA
Mupirocin NDC 70166-355
Mupirocin 20 mg/g · Ointment · Topical · Lohxa
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70166-355-10 | 70166035510 | 100 TUBE in 1 CARTON (70166-355-10) / 1 g in 1 TUBEMarketed from May 26, 2018 | |
| 70166-355-50 | 70166035550 | 50 TUBE in 1 CARTON (70166-355-50) / 1 g in 1 TUBEMarketed from Mar 25, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Mupirocin
- Generic name (nonproprietary)
- mupirocin
- Active ingredients
- Mupirocin — 20 mg/g
- Dosage form
- Ointment
- Route
- Topical
- Labeler
- Lohxa
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 065170
- Marketing start
- Listing expires
- Other FDA classes
- RNA Synthetase Inhibitors (Mechanism)
- Identifiers
- Product ID 70166-355_313090ef-ad58-1103-e063-6394a90a7d75SPL ID 313090ef-ad58-1103-e063-6394a90a7d75SPL set ID 6d59e35c-b262-7940-e053-2991aa0a8908RxCUI 106346UNII D0GX863OA5
- Pharmacologic class
- RNA Synthetase Inhibitor Antibacterial
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470166035510followed by a unit qualifier and the quantityPackage 70166-0355-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Mupirocin Ointment USP, 2% is indicated for the topical treatment of impetigo due to susceptible isolates of Staphylococcus aureus (S. aureus) and Streptococcus pyogenes (S. pyogenes) . Mupirocin ointment is an RNA synthetase inhibitor antibacterial indicated for the topical treatment of impetigo due to susceptible isolates of Staphylococcus aureus and Streptococcus pyogenes . ( 1 )
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 065170
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | Sportpharm LLC | 85766-207 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | NuCare Pharmaceuticals,Inc. | 68071-4321 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | Proficient Rx LP | 63187-151 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | Sun Pharmaceutical Industries, Inc. | 51672-1312 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | PAI Holdings, LLC dba PAI Pharma | 0121-1076 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | AvPAK | 50268-568 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0254 |