What is NDC 68788-8822?

68788-8822 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 7 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 68788-8822 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-8822Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-8822Add 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
68788-8822-1	6878888220168788882201	100 TABLET in 1 BOTTLE (68788-8822-1)Marketed from Feb 10, 2025
68788-8822-2	6878888220268788882202	20 TABLET in 1 BOTTLE (68788-8822-2)Marketed from Feb 10, 2025
68788-8822-3	6878888220368788882203	30 TABLET in 1 BOTTLE (68788-8822-3)Marketed from Feb 10, 2025
68788-8822-4	6878888220468788882204	40 TABLET in 1 BOTTLE (68788-8822-4)Marketed from Feb 10, 2025
68788-8822-6	6878888220668788882206	60 TABLET in 1 BOTTLE (68788-8822-6)Marketed from Feb 10, 2025
68788-8822-8	6878888220868788882208	120 TABLET in 1 BOTTLE (68788-8822-8)Marketed from Feb 10, 2025
68788-8822-9	6878888220968788882209	90 TABLET in 1 BOTTLE (68788-8822-9)Marketed from Feb 10, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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: Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090200
Marketing start: Feb 10, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 68788-8822_eed9ebd1-c243-4e82-bf4e-5fec370e722eSPL ID eed9ebd1-c243-4e82-bf4e-5fec370e722eSPL set ID eed9ebd1-c243-4e82-bf4e-5fec370e722eRxCUI 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

N468788882201 followed by a unit qualifier and the quantity

Package 68788-8822-01. 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 10, 2025.

Indications (excerpt from the label)

INDICATIONS & 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 68788-8822

What is NDC 68788-8822?: 68788-8822 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 7 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?: Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 090200

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

FDA NDC Directory listings under ANDA 090200
Product	Strength	Form · route	Labeler	Product NDC
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-533
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-534
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	A-S Medication Solutions	50090-0182
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	A-S Medication Solutions	50090-0183
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	A-S Medication Solutions	50090-0184
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	A-S Medication Solutions	50090-1781
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	A-S Medication Solutions	50090-1783
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	AvPAK	50268-520
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	AvPAK	50268-521
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Northwind Health Company, LLC	51655-574
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Northwind Health Company, LLC	51655-575
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2129
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2130
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	American Health Packaging	60687-559
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	American Health Packaging	60687-568
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	DIRECT RX	61919-368
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Proficient Rx LP	63187-019
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Proficient Rx LP	63187-087
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Bryant Ranch Prepack	63629-1622
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-146

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