What is NDC 68382-051?

68382-051 is the product NDC for meloxicam, Meloxicam 15 mg/1 tablet, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

Zydus Pharmaceuticals USA Inc., NDC labeler code 68382. 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?

147 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 68382-051 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68382-051Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68382-0051Add 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
68382-051-01	6838200510168382005101	100 TABLET in 1 BOTTLE (68382-051-01)Marketed from Jul 19, 2006
68382-051-05	6838200510568382005105	500 TABLET in 1 BOTTLE (68382-051-05)Marketed from Jul 19, 2006
68382-051-16	6838200511668382005116	90 TABLET in 1 BOTTLE (68382-051-16)Marketed from Jul 19, 2006
68382-051-40	6838200514068382005140	5000 TABLET in 1 BOTTLE (68382-051-40)Marketed from Jul 19, 2006
68382-051-77	6838200517768382005177	10 BLISTER PACK in 1 CARTON (68382-051-77) / 10 TABLET in 1 BLISTER PACK (68382-051-30)Marketed from Jul 19, 2006

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: Zydus Pharmaceuticals USA Inc.NDC labeler code 68382
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077921
Marketing start: Jul 19, 2006
Listing expires: Dec 31, 2027
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 68382-051_87e6ffb9-5a3c-4579-bf50-db901cbdeca9SPL ID 87e6ffb9-5a3c-4579-bf50-db901cbdeca9SPL set ID 6c015f72-5ce3-4f56-8237-776fc2165b0cRxCUI 152695, 311486UNII 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

N468382005101 followed by a unit qualifier and the quantity

Package 68382-0051-01. 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

Current FDA label (SPL), effective Oct 1, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Meloxicam Tablets are 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 co…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68382-051

What is NDC 68382-051?: 68382-051 is the product NDC for meloxicam, Meloxicam 15 mg/1 tablet, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 5 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?: Zydus Pharmaceuticals USA Inc., NDC labeler code 68382. 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?: 147 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 148 meloxicam NDCs

Other NDCs under ANDA 077921

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

FDA NDC Directory listings under ANDA 077921
Product	Strength	Form · route	Labeler	Product NDC
meloxicam	Meloxicam 15 mg/1	TabletOral	REMEDYREPACK INC.	70518-1828
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Coupler LLC	67046-0057
meloxicam	Meloxicam 7.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-3023
meloxicam	Meloxicam 15 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3030
meloxicam	Meloxicam 7.5 mg/1	TabletOral	A-S Medication Solutions	50090-7495
meloxicam	Meloxicam 15 mg/1	TabletOral	PHOENIX RX LLC	85509-1051
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-2080
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-516
Meloxicam	Meloxicam 15 mg/1	TabletOral	American Health Packaging	60687-199
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-129
meloxicam	Meloxicam 15 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-130
Meloxicam	Meloxicam 7.5 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0042
Meloxicam	Meloxicam 15 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0045
meloxicam	Meloxicam 15 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-580
meloxicam	Meloxicam 15 mg/1	TabletOral	Coupler LLC	67046-0891
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7726
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	68382-050
meloxicam	Meloxicam 15 mg/1	TabletOral	Redpharm Drug	67296-1460
meloxicam	Meloxicam 7.5 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-448
meloxicam	Meloxicam 7.5 mg/1	TabletOral	Zydus Lifesciences Limited	65841-050

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