NDC codes

FDA NDC Directory
Product NDC (as listed)72578-130Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72578-0130Add 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
72578-130-0172578013001725780130011 TUBE in 1 CARTON (72578-130-01) / 15 g in 1 TUBEMarketed from Oct 10, 2026
72578-130-0672578013006725780130061 TUBE in 1 CARTON (72578-130-06) / 30 g in 1 TUBEMarketed from Oct 10, 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 calcium — 20 mg/g
Dosage form
Cream
Route
Topical
Labeler
Viona Pharmaceuticals IncNDC labeler code 72578
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218361
Marketing start
Listing expires
Other FDA classes
RNA Synthetase Inhibitors (Mechanism)
Identifiers
Product ID 72578-130_a8cfad1c-cbde-492b-935a-5b362bafe3aeSPL ID a8cfad1c-cbde-492b-935a-5b362bafe3ae
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

N472578013001 followed by a unit qualifier and the quantity

Package 72578-0130-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 72578-130

What is NDC 72578-130?
72578-130 is the product NDC for Mupirocin, Mupirocin calcium 20 mg/g cream, listed with the FDA by Viona Pharmaceuticals Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Mupirocin.
What is the active ingredient?
Mupirocin calcium.
Who is the labeler?
Viona Pharmaceuticals Inc, NDC labeler code 72578. 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 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
Mupirocinmupirocin calciumMupirocin calcium 20 mg/gCreamTopicalREMEDYREPACK INC.70518-377470518-3774-00

All 43 Mupirocin NDCs

Other NDCs under ANDA 218361

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

FDA NDC Directory listings under ANDA 218361
ProductStrengthForm · routeLabelerProduct NDC
MupirocinMupirocin calcium 20 mg/gCreamTopicalZydus Lifesciences Limited70771-1981

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