What is NDC 71335-2305?

71335-2305 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 71335-2305 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2305Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2305Add 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
71335-2305-0	7133523050071335230500	14 TABLET in 1 BOTTLE (71335-2305-0)Marketed from Apr 3, 2024
71335-2305-1	7133523050171335230501	20 TABLET in 1 BOTTLE (71335-2305-1)Marketed from Apr 3, 2024
71335-2305-2	7133523050271335230502	30 TABLET in 1 BOTTLE (71335-2305-2)Marketed from Dec 15, 2023
71335-2305-3	7133523050371335230503	40 TABLET in 1 BOTTLE (71335-2305-3)Marketed from Apr 3, 2024
71335-2305-4	7133523050471335230504	120 TABLET in 1 BOTTLE (71335-2305-4)Marketed from Nov 27, 2023
71335-2305-5	7133523050571335230505	60 TABLET in 1 BOTTLE (71335-2305-5)Marketed from Dec 28, 2023
71335-2305-6	7133523050671335230506	90 TABLET in 1 BOTTLE (71335-2305-6)Marketed from Nov 16, 2023
71335-2305-7	7133523050771335230507	112 TABLET in 1 BOTTLE (71335-2305-7)Marketed from Apr 3, 2024
71335-2305-8	7133523050871335230508	21 TABLET in 1 BOTTLE (71335-2305-8)Marketed from Apr 3, 2024
71335-2305-9	7133523050971335230509	84 TABLET in 1 BOTTLE (71335-2305-9)Marketed from Apr 3, 2024

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 040489
Marketing start: Aug 15, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 71335-2305_c72101c6-a445-4fb2-aa92-54eb626ad030SPL ID c72101c6-a445-4fb2-aa92-54eb626ad030SPL set ID 3f8aed5d-ba8d-4c32-872b-08ab15240cc1RxCUI 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

N471335230500 followed by a unit qualifier and the quantity

Package 71335-2305-00. 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 Jun 10, 2026.

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 71335-2305

What is NDC 71335-2305?: 71335-2305 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 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 500 mg/1	TabletOral	DirectRx	72189-284
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Doc Rx	69306-510
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Asclemed USA, Inc.	76420-626
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-397
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-398
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Asclemed USA, Inc.	76420-638
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Preferred Pharmaceuticals, Inc	68788-7973
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7980
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Asclemed USA, Inc.	76420-258
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	53401-035
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Asclemed USA, Inc.	76420-667
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 500 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-611
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-612
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Proficient Rx LP	82804-954
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Proficient Rx LP	82804-955
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	REGIMED MEDICAL	25685-240
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Proficient Rx LP	82804-121
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-725

Showing 20 of 39.