What is NDC 70771-1981?

70771-1981 is the product NDC for Mupirocin, Mupirocin calcium 20 mg/g cream, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 70771. 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 70771-1981 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1981Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1981Add 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
70771-1981-1	7077119810170771198101	1 TUBE in 1 CARTON (70771-1981-1) / 15 g in 1 TUBEMarketed from Oct 10, 2026
70771-1981-2	7077119810270771198102	1 TUBE in 1 CARTON (70771-1981-2) / 30 g in 1 TUBEMarketed from Oct 10, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218361
Marketing start: Oct 10, 2026
Listing expires: Dec 31, 2027
Other FDA classes: RNA Synthetase Inhibitors (Mechanism)
Identifiers: Product ID 70771-1981_93a19ca4-ca3b-4338-917f-8c0920628574SPL ID 93a19ca4-ca3b-4338-917f-8c0920628574
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

N470771198101 followed by a unit qualifier and the quantity

Package 70771-1981-01. 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 70771-1981

What is NDC 70771-1981?: 70771-1981 is the product NDC for Mupirocin, Mupirocin calcium 20 mg/g cream, listed with the FDA by Zydus Lifesciences Limited. 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?: Zydus Lifesciences Limited, NDC labeler code 70771. 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	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
Mupirocinmupirocin calcium	Mupirocin calcium 20 mg/g	CreamTopical	REMEDYREPACK INC.	70518-3774	70518-3774-00

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
Product	Strength	Form · route	Labeler	Product NDC
Mupirocin	Mupirocin calcium 20 mg/g	CreamTopical	Viona Pharmaceuticals Inc	72578-130