What is NDC 85509-2910?

85509-2910 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by PHOENIX RX LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.

PHOENIX RX LLC, NDC labeler code 85509. 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 85509-2910 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)85509-2910Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85509-2910Add 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
85509-2910-1	85509291001	100 TABLET in 1 BOTTLE (85509-2910-1)Marketed from Feb 13, 2026
85509-2910-3	85509291003	30 TABLET in 1 BOTTLE (85509-2910-3)Marketed from Feb 13, 2026
85509-2910-6	85509291006	60 TABLET in 1 BOTTLE (85509-2910-6)Marketed from Feb 13, 2026
85509-2910-9	85509291009	90 TABLET in 1 BOTTLE (85509-2910-9)Marketed from Feb 13, 2026

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: PHOENIX RX LLCNDC labeler code 85509
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040489
Marketing start: May 22, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 85509-2910_4abc30c4-d454-3908-e063-6394a90a555bSPL ID 4abc30c4-d454-3908-e063-6394a90a555bSPL set ID 4abc29e9-a0cc-06cf-e063-6294a90ad874RxCUI 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

N485509291001 followed by a unit qualifier and the quantity

Package 85509-2910-01. 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 13, 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 85509-2910

What is NDC 85509-2910?: 85509-2910 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by PHOENIX RX LLC. It has 4 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?: PHOENIX RX LLC, NDC labeler code 85509. 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 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 750 mg/1	TabletOral	ASCLEMED USA INC.	87063-689
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Proficient Rx LP	82804-121
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Asclemed USA, Inc.	76420-626
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Bryant Ranch Prepack	71335-2305
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Asclemed USA, Inc.	76420-638
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Asclemed USA, Inc.	76420-258
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Asclemed USA, Inc.	76420-667
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Doc Rx	69306-500
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Doc Rx	69306-510
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0490
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	53401-035
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Preferred Pharmaceuticals, Inc	68788-7973
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7980
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-3105
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	A-S Medication Solutions	50090-5907
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Direct_rx	72189-665
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Medsource Pharmaceuticals	45865-242
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-2383
Methocarbamol	Methocarbamol 750 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-725
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0283

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