What is NDC 63187-151?

63187-151 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.

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?

42 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Mupirocin NDC 63187-151 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-151Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0151Add 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 NDC	11-digit (billing)	Package	Copy
63187-151-22	6318701512263187015122	1 TUBE in 1 CARTON (63187-151-22) / 22 g in 1 TUBEMarketed from Sep 1, 2014

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 065170
Marketing start: Sep 23, 2005
Listing expires: Dec 31, 2027
Other FDA classes: RNA Synthetase Inhibitors (Mechanism)
Identifiers: Product ID 63187-151_a22d9ce1-ccc1-4955-939c-b74e110cffa5SPL ID a22d9ce1-ccc1-4955-939c-b74e110cffa5SPL set ID d8766748-6b53-4673-a3ee-5cd8a4301647RxCUI 106346UNII D0GX863OA5UPC 0363187151225
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

N463187015122 followed by a unit qualifier and the quantity

Package 63187-0151-22. 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 Jan 1, 2023.

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 63187-151

What is NDC 63187-151?: 63187-151 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?: 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mupirocin	Mupirocin calcium 20 mg/g	CreamTopical	Zydus Lifesciences Limited	70771-1981	70771-1981-0170771-1981-02
Mupirocin	Mupirocin calcium 20 mg/g	CreamTopical	Viona Pharmaceuticals Inc	72578-130	72578-0130-0172578-0130-06
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	PAI Holdings, LLC dba PAI Pharma	0121-1076	00121-1076-50
Mupirocinmupirocin ointment	Mupirocin 20 mg/g	OintmentTopical	Kesin Pharma Corporation	81033-032	81033-0032-5081033-0032-99
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Encube Ethicals, Inc.	21922-073	21922-0073-0421922-0073-0521922-0073-25
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Redpharm Drug	67296-2211	67296-2211-01
Mupirocin	Mupirocin calcium 20 mg/g	CreamTopical	Alembic Pharmaceuticals Limited	46708-624	46708-0624-1546708-0624-30
mupirocin	Mupirocin 20 mg/g	OintmentTopical	St. Mary's Medical Park Pharmacy	60760-960	60760-0960-22
mupirocin	Mupirocin 20 mg/g	OintmentTopical	Preferred Pharmaceuticals Inc.	68788-8642	68788-8642-02
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Preferred Pharmaceuticals Inc.	68788-8534	68788-8534-02

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
Product	Strength	Form · route	Labeler	Product NDC
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	Sun Pharmaceutical Industries, Inc.	51672-1312
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	NuCare Pharmaceuticals,Inc.	68071-4321
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Lohxa	70166-355
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Advanced Rx Pharmacy of Tennessee, LLC	80425-0254
Mupirocin	Mupirocin 20 mg/g	OintmentTopical	Sportpharm LLC	85766-207