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
85766-207-1585766020715857660207151 TUBE in 1 CARTON (85766-207-15) / 15 g in 1 TUBEMarketed from May 12, 2026
85766-207-2285766020722857660207221 TUBE in 1 CARTON (85766-207-22) / 22 g in 1 TUBEMarketed from May 12, 2026
85766-207-3085766020730857660207301 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
Labeler
Sportpharm LLCNDC labeler code 85766
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)

About NDC 85766-207

What is NDC 85766-207?
85766-207 is the product NDC for Mupirocin, Mupirocin 20 mg/g ointment, listed with the FDA by Sportpharm LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Mupirocin.
What is the active ingredient?
Mupirocin.
Who is the labeler?
Sportpharm LLC, NDC labeler code 85766. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mupirocin?
42 other product NDCs are listed under this name. See all Mupirocin NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Mupirocin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
MupirocinMupirocin calcium 20 mg/gCreamTopicalZydus Lifesciences Limited70771-198170771-1981-0170771-1981-02
MupirocinMupirocin calcium 20 mg/gCreamTopicalViona Pharmaceuticals Inc72578-13072578-0130-0172578-0130-06
MupirocinMupirocin 20 mg/gOintmentTopicalPAI Holdings, LLC dba PAI Pharma0121-107600121-1076-50
Mupirocinmupirocin ointmentMupirocin 20 mg/gOintmentTopicalKesin Pharma Corporation81033-03281033-0032-5081033-0032-99
MupirocinMupirocin 20 mg/gOintmentTopicalEncube Ethicals, Inc.21922-07321922-0073-0421922-0073-0521922-0073-25
MupirocinMupirocin 20 mg/gOintmentTopicalRedpharm Drug67296-221167296-2211-01
MupirocinMupirocin calcium 20 mg/gCreamTopicalAlembic Pharmaceuticals Limited46708-62446708-0624-1546708-0624-30
mupirocinMupirocin 20 mg/gOintmentTopicalSt. Mary's Medical Park Pharmacy60760-96060760-0960-22
mupirocinMupirocin 20 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-864268788-8642-02
MupirocinMupirocin 20 mg/gOintmentTopicalPreferred Pharmaceuticals Inc.68788-853468788-8534-02

All 43 Mupirocin NDCs

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/gOintmentTopicalPAI Holdings, LLC dba PAI Pharma0121-1076
MupirocinMupirocin 20 mg/gOintmentTopicalAvPAK50268-568
MupirocinMupirocin 20 mg/gOintmentTopicalSun Pharmaceutical Industries, Inc.51672-1312
MupirocinMupirocin 20 mg/gOintmentTopicalProficient Rx LP63187-151
MupirocinMupirocin 20 mg/gOintmentTopicalNuCare Pharmaceuticals,Inc.68071-4321
MupirocinMupirocin 20 mg/gOintmentTopicalLohxa70166-355
MupirocinMupirocin 20 mg/gOintmentTopicalAdvanced Rx Pharmacy of Tennessee, LLC80425-0254

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