What is NDC 80425-0138?

80425-0138 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, film coated, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. 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 80425-0138 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)80425-0138Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80425-0138Add 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
80425-0138-1	80425013801	60 TABLET, FILM COATED in 1 BOTTLE (80425-0138-1)Marketed from Jan 15, 2018
80425-0138-2	80425013802	90 TABLET, FILM COATED in 1 BOTTLE (80425-0138-2)Marketed from Jan 15, 2018

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, Film coated
Route: Oral
Labeler: Advanced Rx Pharmacy of Tennessee, LLCNDC labeler code 80425
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208507
Marketing start: Jan 15, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 80425-0138_2a998081-6432-8228-e063-6294a90adc3dSPL ID 2a998081-6432-8228-e063-6294a90adc3dSPL set ID c06c4a63-491c-baa2-e053-2a95a90a09ffRxCUI 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

N480425013801 followed by a unit qualifier and the quantity

Package 80425-0138-01. 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 Dec 31, 2024.

Indications (excerpt from the label)

Indications and Usage Section Methocarbamol Tablets USP, 500 mg and 750 mg 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 80425-0138

What is NDC 80425-0138?: 80425-0138 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, film coated, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. 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?: Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. 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 208507

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

FDA NDC Directory listings under ANDA 208507
Product	Strength	Form · route	Labeler	Product NDC
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0171
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0828
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	UNICHEM PHARMACEUTICALS (USA), INC.	76385-124
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	UNICHEM PHARMACEUTICALS (USA), INC.	76385-123
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-285
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0970
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Asclemed USA, Inc.	76420-040
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-021
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-012
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-022
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-041
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-103
Methocarbamol	Methocarbamol 750 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-174
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-4793
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-110
Methocarbamol	Methocarbamol 500 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-3578