What is NDC 63187-087?

63187-087 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 6 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 63187. 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?

197 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 63187-087 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-087Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0087Add 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
63187-087-00	63187008700	100 TABLET in 1 BOTTLE (63187-087-00)Marketed from Apr 1, 2014
63187-087-20	63187008720	20 TABLET in 1 BOTTLE (63187-087-20)Marketed from Apr 1, 2014
63187-087-30	63187008730	30 TABLET in 1 BOTTLE (63187-087-30)Marketed from Apr 1, 2014
63187-087-40	63187008740	40 TABLET in 1 BOTTLE (63187-087-40)Marketed from Apr 1, 2014
63187-087-60	63187008760	60 TABLET in 1 BOTTLE (63187-087-60)Marketed from Apr 1, 2014
63187-087-90	63187008790	90 TABLET in 1 BOTTLE (63187-087-90)Marketed from Apr 1, 2014

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: Proficient Rx LPNDC labeler code 63187
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090200
Marketing start: Mar 20, 2013
Listing expires: Dec 31, 2026
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 63187-087_87a7950f-b987-4ee0-901e-49b19054707bSPL ID 87a7950f-b987-4ee0-901e-49b19054707bSPL set ID 10ae354f-94a4-4d4e-bccc-ea189726b7ceRxCUI 197943, 197944UNII 125OD7737XUPC 0363187087302
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

N463187008700 followed by a unit qualifier and the quantity

Package 63187-0087-00. 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, 2022.

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 63187-087

What is NDC 63187-087?: 63187-087 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 6 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?: Proficient Rx LP, NDC labeler code 63187. 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?: 197 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)
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
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-057	87441-0057-01
Methocarbamolmethocarbamol tablets	Methocarbamol 500 mg/1	Tablet, CoatedOral	Coupler LLC	67046-0538	67046-0538-03
Methocarbamol	Methocarbamol 100 mg/mL	InjectionIntramuscular, Intravenous, Intravenous	JVET PHARMACEUTICALS LLC	86211-114	86211-0114-10

All 198 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	Bryant Ranch Prepack	63629-1622
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-146
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	66267-803

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