What is NDC 70518-4472?

70518-4472 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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 70518-4472 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4472Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4472Add 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	Copy
70518-4472-0	7051844720070518447200	90 TABLET in 1 BOTTLE, PLASTIC (70518-4472-0)Marketed from Sep 9, 2025
70518-4472-1	7051844720170518447201	60 TABLET in 1 BOTTLE, PLASTIC (70518-4472-1)Marketed from Sep 9, 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 — 750 mg/1
Dosage form: Tablet
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 086988
Marketing start: Sep 9, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 70518-4472_5b38e05a-5d95-0e86-e063-6294a90aca49SPL ID 5b38e05a-5d95-0e86-e063-6294a90aca49
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

N470518447200 followed by a unit qualifier and the quantity

Package 70518-4472-00. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70518-4472

What is NDC 70518-4472?: 70518-4472 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 2 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?: REMEDYREPACK INC., NDC labeler code 70518. 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 086988

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

FDA NDC Directory listings under ANDA 086988
Product	Strength	Form · route	Labeler	Product NDC
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Major Pharmaceuticals	0904-7057
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Major Pharmaceuticals	0904-7058
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Solco Healthcare LLC	43547-226
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Solco Healthcare LLC	43547-405
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-467
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Golden State Medical Supply, Inc.	51407-468
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2334
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2335
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Proficient Rx LP	63187-130
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Bryant Ranch Prepack	63629-8995
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Bryant Ranch Prepack	71335-1727
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-598