What is NDC 82461-723?

82461-723 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, film coated, listed with the FDA by Medcore LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Medcore LLC, NDC labeler code 82461. 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 82461-723 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)82461-723Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82461-0723Add 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
82461-723-90	8246107239082461072390	90 TABLET, FILM COATED in 1 BOTTLE (82461-723-90)Marketed from Jul 31, 2026

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: Medcore LLCNDC labeler code 82461
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212623
Marketing start: Jul 31, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 82461-723_1745e58f-e6fb-43d8-a738-74a2cc80db48SPL ID 1745e58f-e6fb-43d8-a738-74a2cc80db48SPL set ID 1a6b7327-fd42-4de0-bd0d-2dd478502d52RxCUI 197943, 197944UNII 125OD7737XUPC 0382461723903, 0382461722906
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

N482461072390 followed by a unit qualifier and the quantity

Package 82461-0723-90. 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 Jul 29, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Methocarbamol Tablets, USP 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 82461-723

What is NDC 82461-723?: 82461-723 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, film coated, listed with the FDA by Medcore LLC. It has 1 package NDC, 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?: Medcore LLC, NDC labeler code 82461. 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
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
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-057	87441-0057-01

All 201 Methocarbamol NDCs

Other NDCs under ANDA 212623

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

FDA NDC Directory listings under ANDA 212623
Product	Strength	Form · route	Labeler	Product NDC
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-722
Methocarbamol Tablets, USP, 500 mgmethocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Marlex Pharmaceuticals, Inc.	10135-722
Methocarbamol Tablets, USP, 500 mgmethocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Granulation Technology, Inc.	63561-0173
Methocarbamol Tablets, USP, 500 mgmethocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-2487
Methocarbamol Tablets, USP, 500 mgmethocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-481
Methocarbamol Tablets, USP, 500 mgmethocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-499
Methocarbamol Tablets, USP, 750 mgmethocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Marlex Pharmaceuticals, Inc.	10135-723
Methocarbamol Tablets, USP, 750 mgmethocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Granulation Technology, Inc.	63561-0174
Methocarbamol Tablets, USP, 750 mgmethocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-2488
Methocarbamol Tablets, USP, 750 mgmethocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-521