What is NDC 76420-667?

76420-667 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by Asclemed USA, Inc.. It has 4 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 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 76420-667 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)76420-667Labeler and product segments. Claims need a package NDC.

Product NDC at billing width76420-0667Add 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
76420-667-01	7642006670176420066701	100 TABLET in 1 BOTTLE (76420-667-01)Marketed from Feb 8, 2024
76420-667-30	7642006673076420066730	30 TABLET in 1 BOTTLE (76420-667-30)Marketed from Feb 8, 2024
76420-667-60	7642006676076420066760	60 TABLET in 1 BOTTLE (76420-667-60)Marketed from Feb 8, 2024
76420-667-90	7642006679076420066790	90 TABLET in 1 BOTTLE (76420-667-90)Marketed from Feb 8, 2024

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 — 500 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 040489
Marketing start: Jan 1, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 76420-667_10d86b36-7cd4-9296-e063-6394a90a4166SPL ID 10d86b36-7cd4-9296-e063-6394a90a4166SPL set ID 1637e18d-d9f9-4171-99e6-4b866d821c87RxCUI 197943UNII 125OD7737X
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

N476420066701 followed by a unit qualifier and the quantity

Package 76420-0667-01. 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 Feb 7, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Methocarbamol is 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 76420-667

What is NDC 76420-667?: 76420-667 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by Asclemed USA, Inc.. It has 4 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?: 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 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 040489

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

FDA NDC Directory listings under ANDA 040489
Product	Strength	Form · route	Labeler	Product NDC
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Asclemed USA, Inc.	76420-638
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	ASCLEMED USA INC.	87063-135
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	HAWAII REPACK, INC.	85534-0057
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Preferred Pharmaceuticals, Inc	68788-7973
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	DirectRx	72189-284
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7980
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Asclemed USA, Inc.	76420-626
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-429
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-428
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	53401-035
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Asclemed USA, Inc.	76420-258
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-611
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-612
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-725
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	REGIMED MEDICAL	25685-240
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3636
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Proficient Rx LP	82804-954
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Proficient Rx LP	82804-955
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	ASCLEMED USA INC.	87063-689
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Proficient Rx LP	82804-121

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