NDC codes

FDA NDC Directory
Product NDC (as listed)63187-525Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0525Add 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
63187-525-22631870525221 TUBE in 1 CARTON (63187-525-22) / 22 g in 1 TUBEMarketed from Nov 7, 2003

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
Proficient Rx LPNDC labeler code 63187
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 065085
Marketing start
Listing expires
Other FDA classes
RNA Synthetase Inhibitors (Mechanism)
Identifiers
Product ID 63187-525_75ec5f25-865b-455a-b8d6-c942abce985aSPL ID 75ec5f25-865b-455a-b8d6-c942abce985aSPL set ID cbb18010-f3b5-4ed7-8c03-c9203f0e360eRxCUI 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

N463187052522 followed by a unit qualifier and the quantity

Package 63187-0525-22. 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)

INDICATIONS AND USAGE Mupirocin ointment USP, 2% is indicated for the topical treatment of impetigo due to: S. aureus and S. pyogenes .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-525

What is NDC 63187-525?
63187-525 is the product NDC for Mupirocin, Mupirocin 20 mg/g ointment, listed with the FDA by Proficient Rx LP. It has 1 package NDC, 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?
Proficient Rx LP, NDC labeler code 63187. 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?
40 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 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
MupirocinMupirocin 20 mg/gOintmentTopicalAdvanced Rx Pharmacy of Tennessee, LLC80425-024680425-0246-01

All 41 Mupirocin NDCs

Other NDCs under ANDA 065085

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

FDA NDC Directory listings under ANDA 065085
ProductStrengthForm · routeLabelerProduct NDC
MupirocinMupirocin 20 mg/gOintmentTopicalTeva Pharmaceuticals USA, Inc.0093-1010
MupirocinMupirocin 20 mg/gOintmentTopicalDIRECT RX61919-158
MupirocinMupirocin 20 mg/gOintmentTopicalAdvanced Rx Pharmacy of Tennessee, LLC80425-0246

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