What is NDC 76420-039?

76420-039 is the product NDC for meloxicam, Meloxicam 15 mg/1 tablet, listed with the FDA by Asclemed USA, Inc.. It has 11 package NDCs, shown above in 10- and 11-digit form.

Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for meloxicam?

148 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

meloxicam NDC 76420-039 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)76420-039Labeler and product segments. Claims need a package NDC.

Product NDC at billing width76420-0039Add 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
76420-039-00	76420003900	1000 TABLET in 1 BOTTLE (76420-039-00)Marketed from Feb 7, 2025
76420-039-01	76420003901	100 TABLET in 1 BOTTLE (76420-039-01)Marketed from Feb 7, 2025
76420-039-05	76420003905	500 TABLET in 1 BOTTLE (76420-039-05)Marketed from Feb 7, 2025
76420-039-07	76420003907	7 TABLET in 1 BOTTLE (76420-039-07)Marketed from Mar 31, 2023
76420-039-10	76420003910	10 TABLET in 1 BOTTLE (76420-039-10)Marketed from Sep 4, 2020
76420-039-14	76420003914	14 TABLET in 1 BOTTLE (76420-039-14)Marketed from Sep 2, 2023
76420-039-20	76420003920	20 TABLET in 1 BOTTLE (76420-039-20)Marketed from Sep 2, 2023
76420-039-30	76420003930	30 TABLET in 1 BOTTLE (76420-039-30)Marketed from Feb 15, 2020
76420-039-55	76420003955	5000 TABLET in 1 BOTTLE (76420-039-55)Marketed from Feb 7, 2025
76420-039-60	76420003960	60 TABLET in 1 BOTTLE (76420-039-60)Marketed from Feb 15, 2020
76420-039-90	76420003990	90 TABLET in 1 BOTTLE (76420-039-90)Marketed from Sep 4, 2020

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): meloxicam
Generic name (nonproprietary): meloxicam
Active ingredients: Meloxicam — 15 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Asclemed USA, Inc.NDC labeler code 76420
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077927
Marketing start: Mar 7, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 76420-039_2d871eb9-b21b-4113-e063-6294a90a118cSPL ID 2d871eb9-b21b-4113-e063-6294a90a118cSPL set ID 4dc34489-cbb6-4e57-a2cc-a274209456f3RxCUI 152695UNII VG2QF83CGL
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N476420003900 followed by a unit qualifier and the quantity

Package 76420-0039-00. 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 Feb 6, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Meloxicam tablets are a non-steroidal anti-inflammatory drug indicated for: Osteoarthritis (OA) ( 1.1 ) Rheumatoid Arthritis (RA) ( 1.2 ) Juvenile Rheumatoid Arthritis (JRA) in patients who weigh ≥60 kg ( 1.3 ) 1.1 Osteoarthritis (OA) Meloxicam tablets are indicated for relief of the signs and symptoms of osteoarthritis [ see Clinical Studies ( 14.1 ) ]. 1.2 Rheumatoid Arthritis (RA) Meloxicam tablets are indicated for relief of the signs and symptoms of rheumatoid arthritis [ see Clinical Studies ( 14.1 ) ]. 1.3 Juvenile Rheumatoid Arthritis (JRA) Pauciarticular and Polyarticular Course Meloxicam tablets are indicated for relief of the signs and symptoms of pauciarticular or polyarticular c…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 76420-039

What is NDC 76420-039?: 76420-039 is the product NDC for meloxicam, Meloxicam 15 mg/1 tablet, listed with the FDA by Asclemed USA, Inc.. It has 11 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: meloxicam.
What is the active ingredient?: Meloxicam.
Who is the labeler?: Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for meloxicam?: 148 other product NDCs are listed under this name. See all meloxicam 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 meloxicam NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Meloxicam	Meloxicam 7.5 mg/1	TabletOral	Direct_Rx	72189-683	72189-0683-3072189-0683-6072189-0683-72+1 more
Meloxicam	Meloxicam 15 mg/1	TabletOral	Direct_Rx	72189-684	72189-0684-30
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Coupler LLC	67046-1342	67046-1342-03
Meloxicam	Meloxicam 15 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0584	80425-0584-0180425-0584-0280425-0584-03
Meloxicam	Meloxicam 15 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0585	80425-0585-0180425-0585-0280425-0585-03
Meloxicam	Meloxicam 15 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0586	80425-0586-0180425-0586-0280425-0586-03
meloxicam	Meloxicam 15 mg/1	TabletOral	Coupler LLC	67046-0891	67046-0891-03
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Coupler LLC	67046-0057	67046-0057-03
Meloxicam	Meloxicam 7.5 mg/1	TabletOral	Medcore LLC	82461-719	82461-0719-30
Meloxicam	Meloxicam 7.5 mg/1	TabletOral	AiPing Pharmaceutical, Inc	11788-046	11788-0046-0111788-0046-0511788-0046-10

All 149 meloxicam NDCs

Other NDCs under ANDA 077927

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

FDA NDC Directory listings under ANDA 077927
Product	Strength	Form · route	Labeler	Product NDC
meloxicam	Meloxicam 7.5 mg/1	TabletOral	QPharma, Inc.	42708-093
Meloxicam	Meloxicam 7.5 mg/1	TabletOral	Exelan Pharmaceuticals Inc.	76282-152
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Coupler LLC	67046-1342
Meloxicam	Meloxicam 15 mg/1	TabletOral	Exelan Pharmaceuticals Inc.	76282-153
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8758
meloxicam	Meloxicam 15 mg/1	TabletOral	REMEDYREPACK INC.	70518-0394
meloxicam	Meloxicam 15 mg/1	TabletOral	Bryant Ranch Prepack	63629-3328
meloxicam	Meloxicam 15 mg/1	TabletOral	Sportpharm LLC	85766-036
meloxicam	Meloxicam 15 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-1993
meloxicam	Meloxicam 7.5 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-1994
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-124
meloxicam	Meloxicam 15 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-125
meloxicam	Meloxicam 7.5 mg/1	TabletOral	PHOENIX RX LLC	85509-1124
meloxicam	Meloxicam 15 mg/1	TabletOral	PHOENIX RX LLC	85509-1125
meloxicam	Meloxicam 15 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8801
Meloxicam	Meloxicam 15 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-544
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0406
meloxicam	Meloxicam 15 mg/1	TabletOral	Northwind Health Company, LLC	51655-577
Meloxicam	Meloxicam 7.5 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0041
Meloxicam	Meloxicam 15 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0044

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