NDC codes

FDA NDC Directory
Product NDC (as listed)60760-874Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60760-0874Add 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 NDC11-digit (billing)PackageCopy
60760-874-90607600874906076008749090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-874-90)Marketed from Sep 17, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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
St. Mary's Medical Park PharmacyNDC labeler code 60760
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213967
Marketing start
Listing expires
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 60760-874_5bc71001-809c-9aa1-e063-6294a90a67f2SPL ID 5bc71001-809c-9aa1-e063-6294a90a67f2
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

N460760087490 followed by a unit qualifier and the quantity

Package 60760-0874-90. 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 60760-874

What is NDC 60760-874?
60760-874 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, film coated, listed with the FDA by St. Mary's Medical Park Pharmacy. It has 1 package NDC, 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?
St. Mary's Medical Park Pharmacy, NDC labeler code 60760. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Methocarbamolmethocarbamol tabletsMethocarbamol 500 mg/1Tablet, CoatedOralAmerican Health Packaging60687-94560687-0945-01
Methocarbamolmethocarbamol tabletsMethocarbamol 750 mg/1Tablet, CoatedOralAmerican Health Packaging60687-95660687-0956-01
MethocarbamolMethocarbamol 500 mg/1TabletOralREGIMED MEDICAL25685-24025685-0240-10
Methocarbamolmethocarbamol tabletsMethocarbamol 750 mg/1Tablet, CoatedOralCoupler LLC67046-034067046-0340-03
MethocarbamolMethocarbamol 500 mg/1TabletOralCoupler LLC67046-117767046-1177-03
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralMedcore LLC82461-72282461-0722-90
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralMedcore LLC82461-72382461-0723-90
Methocarbamolmethocarbamol tabletsMethocarbamol 500 mg/1Tablet, CoatedOralUnit Dose Solutions, Inc.87441-08687441-0086-01
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-87560760-0875-2860760-0875-4060760-0875-90
MethocarbamolMethocarbamol 500 mg/1TabletOralUnit Dose Solutions, Inc.87441-05787441-0057-01

All 201 Methocarbamol NDCs

Other NDCs under ANDA 213967

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

FDA NDC Directory listings under ANDA 213967
ProductStrengthForm · routeLabelerProduct NDC
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2795
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2794
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8506
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-340
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-341
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8507
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8867
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8876
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralPHOENIX RX LLC85509-1341
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralRedpharm Drug67296-2193
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralSportpharm LLC85766-060
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-3859
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-875
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralAsclemed USA, Inc.87063-040
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralAsclemed USA, Inc.87063-041

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