NDC codes

FDA NDC Directory
Product NDC (as listed)85766-207Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85766-0207Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
85766-207-15857660207151 TUBE in 1 CARTON (85766-207-15) / 15 g in 1 TUBEMarketed from May 12, 2026
85766-207-22857660207221 TUBE in 1 CARTON (85766-207-22) / 22 g in 1 TUBEMarketed from May 12, 2026
85766-207-30857660207301 TUBE in 1 CARTON (85766-207-30) / 30 g in 1 TUBEMarketed from May 12, 2026

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
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 85766-207_519b17d8-7f80-8653-e063-6394a90ad7eaSPL ID 519b17d8-7f80-8653-e063-6394a90ad7eaSPL set ID c70dd5d7-6995-4a3d-b19c-9b4a2cfe3da9RxCUI 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

N485766020715 followed by a unit qualifier and the quantity

Package 85766-0207-15. 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.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 065170

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 065170
ProductStrengthForm · routeLabelerProduct NDC
MupirocinMupirocin 20 mg/gOintmentTopicalNuCare Pharmaceuticals,Inc.68071-4321
MupirocinMupirocin 20 mg/gOintmentTopicalProficient Rx LP63187-151
MupirocinMupirocin 20 mg/gOintmentTopicalSun Pharmaceutical Industries, Inc.51672-1312
MupirocinMupirocin 20 mg/gOintmentTopicalPAI Holdings, LLC dba PAI Pharma0121-1076
MupirocinMupirocin 20 mg/gOintmentTopicalAvPAK50268-568
MupirocinMupirocin 20 mg/gOintmentTopicalAdvanced Rx Pharmacy of Tennessee, LLC80425-0254
MupirocinMupirocin 20 mg/gOintmentTopicalLohxa70166-355

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