NDC codes

FDA NDC Directory
Product NDC (as listed)51655-574Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51655-0574Add 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
51655-574-52516550574525165505745230 TABLET in 1 BOTTLE, PLASTIC (51655-574-52)Marketed from Dec 23, 2020
51655-574-84516550574845165505748414 TABLET in 1 BOTTLE, PLASTIC (51655-574-84)Marketed from Sep 16, 2020

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
Route
Oral
Labeler
Northwind Health Company, LLCNDC labeler code 51655
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090200
Marketing start
Listing expires
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 51655-574_494e36ce-4cbb-e470-e063-6394a90a2955SPL ID 494e36ce-4cbb-e470-e063-6394a90a2955SPL set ID f31ccb09-7a9a-60af-e053-2995a90a6e97RxCUI 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

N451655057452 followed by a unit qualifier and the quantity

Package 51655-0574-52. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 51655-574

What is NDC 51655-574?
51655-574 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by Northwind Health Company, 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?
Northwind Health Company, LLC, NDC labeler code 51655. 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 500 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-87460760-0874-90
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

All 201 Methocarbamol NDCs

Other NDCs under ANDA 090200

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

FDA NDC Directory listings under ANDA 090200
ProductStrengthForm · routeLabelerProduct NDC
MethocarbamolMethocarbamol 500 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-533
MethocarbamolMethocarbamol 750 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-534
MethocarbamolMethocarbamol 500 mg/1TabletOralA-S Medication Solutions50090-0182
MethocarbamolMethocarbamol 500 mg/1TabletOralA-S Medication Solutions50090-0183
MethocarbamolMethocarbamol 500 mg/1TabletOralA-S Medication Solutions50090-0184
MethocarbamolMethocarbamol 750 mg/1TabletOralA-S Medication Solutions50090-1781
MethocarbamolMethocarbamol 750 mg/1TabletOralA-S Medication Solutions50090-1783
MethocarbamolMethocarbamol 500 mg/1TabletOralAvPAK50268-520
MethocarbamolMethocarbamol 750 mg/1TabletOralAvPAK50268-521
MethocarbamolMethocarbamol 750 mg/1TabletOralNorthwind Health Company, LLC51655-575
MethocarbamolMethocarbamol 500 mg/1TabletOralCardinal Health 107, LLC55154-2129
MethocarbamolMethocarbamol 750 mg/1TabletOralCardinal Health 107, LLC55154-2130
MethocarbamolMethocarbamol 500 mg/1TabletOralAmerican Health Packaging60687-559
MethocarbamolMethocarbamol 750 mg/1TabletOralAmerican Health Packaging60687-568
MethocarbamolMethocarbamol 500 mg/1TabletOralDIRECT RX61919-368
MethocarbamolMethocarbamol 750 mg/1TabletOralProficient Rx LP63187-019
MethocarbamolMethocarbamol 500 mg/1TabletOralProficient Rx LP63187-087
MethocarbamolMethocarbamol 500 mg/1TabletOralBryant Ranch Prepack63629-1622
MethocarbamolMethocarbamol 750 mg/1TabletOralNuCare Pharmaceuticals, Inc.66267-146
MethocarbamolMethocarbamol 750 mg/1TabletOralNuCare Pharmaceuticals,Inc.66267-803

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