What is NDC 71335-0251?

71335-0251 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-0251 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0251Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0251Add 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
71335-0251-0	7133502510071335025100	14 TABLET in 1 BOTTLE (71335-0251-0)Marketed from Dec 27, 2021
71335-0251-1	7133502510171335025101	20 TABLET in 1 BOTTLE (71335-0251-1)Marketed from Mar 25, 2019
71335-0251-2	7133502510271335025102	30 TABLET in 1 BOTTLE (71335-0251-2)Marketed from Mar 12, 2018
71335-0251-3	7133502510371335025103	40 TABLET in 1 BOTTLE (71335-0251-3)Marketed from Mar 13, 2018
71335-0251-4	7133502510471335025104	120 TABLET in 1 BOTTLE (71335-0251-4)Marketed from Feb 16, 2018
71335-0251-5	7133502510571335025105	60 TABLET in 1 BOTTLE (71335-0251-5)Marketed from Mar 7, 2018
71335-0251-6	7133502510671335025106	90 TABLET in 1 BOTTLE (71335-0251-6)Marketed from Mar 8, 2018
71335-0251-7	7133502510771335025107	112 TABLET in 1 BOTTLE (71335-0251-7)Marketed from Dec 27, 2021
71335-0251-8	7133502510871335025108	21 TABLET in 1 BOTTLE (71335-0251-8)Marketed from Dec 27, 2021
71335-0251-9	7133502510971335025109	84 TABLET in 1 BOTTLE (71335-0251-9)Marketed from Dec 27, 2021

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 — 750 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
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 71335-0251_31def693-59aa-4029-9f78-ddbb3a5271c2SPL ID 31def693-59aa-4029-9f78-ddbb3a5271c2SPL set ID 3f47c39b-9373-454f-9a4e-ba6dd65dd7a4RxCUI 197944UNII 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

N471335025100 followed by a unit qualifier and the quantity

Package 71335-0251-00. 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 Aug 20, 2024.

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 71335-0251

What is NDC 71335-0251?: 71335-0251 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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 750 mg/1	Tablet, Film coatedOral	Medcore LLC	82461-723	82461-0723-90
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

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 750 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	66267-803
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-057
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	AvPAK	50268-520
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	AvPAK	50268-521
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	Preferred Pharmaceuticals Inc.	68788-8822
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	XLCare Pharmaceuticals Inc.	72865-234
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Northwind Health Company, LLC	51655-574
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	XLCare Pharmaceuticals Inc.	72865-233
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Northwind Health Company, LLC	51655-575
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0275
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	DIRECT RX	61919-368
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	A-S Medication Solutions	50090-0184
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Bryant Ranch Prepack	63629-1622
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-832
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Proficient Rx LP	63187-019
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-833

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