What is NDC 59651-341?

59651-341 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 59651. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Methocarbamol?

200 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Methocarbamol NDC 59651-341 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59651-341Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59651-0341Add 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
59651-341-01	5965103410159651034101	100 TABLET, FILM COATED in 1 BOTTLE (59651-341-01)Marketed from Aug 12, 2020
59651-341-05	5965103410559651034105	500 TABLET, FILM COATED in 1 BOTTLE (59651-341-05)Marketed from Aug 12, 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): Methocarbamol
Generic name (nonproprietary): methocarbamol
Active ingredients: Methocarbamol — 750 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Aurobindo Pharma LimitedNDC labeler code 59651
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213967
Marketing start: Aug 12, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 59651-341_a67f1603-a117-4a69-b4f2-ea348425396eSPL ID a67f1603-a117-4a69-b4f2-ea348425396eSPL set ID f83dd093-ea53-44c1-a40d-682ebc494b62RxCUI 197943, 197944UNII 125OD7737XUPC 0359651340011
Pharmacologic class: Muscle Relaxant

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

N459651034101 followed by a unit qualifier and the quantity

Package 59651-0341-01. 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 Jan 18, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Methocarbamol tablets are indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. The mode of action of methocarbamol has not been clearly identified, but may be related to its sedative properties. Methocarbamol does not directly relax tense skeletal muscles in man.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59651-341

What is NDC 59651-341?: 59651-341 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, film coated, listed with the FDA by Aurobindo Pharma Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Methocarbamol.
What is the active ingredient?: Methocarbamol.
Who is the labeler?: Aurobindo Pharma Limited, NDC labeler code 59651. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Methocarbamol?: 200 other product NDCs are listed under this name. See all Methocarbamol 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 Methocarbamol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Methocarbamolmethocarbamol tablets	Methocarbamol 500 mg/1	Tablet, CoatedOral	American Health Packaging	60687-945	60687-0945-01
Methocarbamolmethocarbamol tablets	Methocarbamol 750 mg/1	Tablet, CoatedOral	American Health Packaging	60687-956	60687-0956-01
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	REGIMED MEDICAL	25685-240	25685-0240-10
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-874	60760-0874-90
Methocarbamolmethocarbamol tablets	Methocarbamol 750 mg/1	Tablet, CoatedOral	Coupler LLC	67046-0340	67046-0340-03
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Coupler LLC	67046-1177	67046-1177-03
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-722	82461-0722-90
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-723	82461-0723-90
Methocarbamolmethocarbamol tablets	Methocarbamol 500 mg/1	Tablet, CoatedOral	Unit Dose Solutions, Inc.	87441-086	87441-0086-01
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-875	60760-0875-2860760-0875-4060760-0875-90

All 201 Methocarbamol NDCs

Other NDCs under ANDA 213967

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

FDA NDC Directory listings under ANDA 213967
Product	Strength	Form · route	Labeler	Product NDC
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2795
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2794
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8506
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-340
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8507
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8867
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8876
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	PHOENIX RX LLC	85509-1341
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Redpharm Drug	67296-2193
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Sportpharm LLC	85766-060
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-3859
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-874
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-875
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Asclemed USA, Inc.	87063-040
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Asclemed USA, Inc.	87063-041