NDC codes

FDA NDC Directory
Product NDC (as listed)87063-689Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87063-0689Add 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
87063-689-1287063068912120 TABLET in 1 BOTTLE (87063-689-12)Marketed from Jun 25, 2026
87063-689-308706306893030 TABLET in 1 BOTTLE (87063-689-30)Marketed from Jun 25, 2026
87063-689-608706306896060 TABLET in 1 BOTTLE (87063-689-60)Marketed from Jun 25, 2026
87063-689-908706306899090 TABLET in 1 BOTTLE (87063-689-90)Marketed from Jun 25, 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 — 750 mg/1
Dosage form
Tablet
Route
Oral
Labeler
ASCLEMED USA INC.NDC labeler code 87063
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040489
Marketing start
Listing expires
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 87063-689_5512a216-a094-2b38-e063-6394a90a86c7SPL ID 5512a216-a094-2b38-e063-6394a90a86c7
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

N487063068912 followed by a unit qualifier and the quantity

Package 87063-0689-12. 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 87063-689

What is NDC 87063-689?
87063-689 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, listed with the FDA by ASCLEMED USA INC.. 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?
ASCLEMED USA INC., NDC labeler code 87063. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
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
MethocarbamolMethocarbamol 500 mg/1TabletOralUnit Dose Solutions, Inc.87441-05787441-0057-01
Methocarbamolmethocarbamol tabletsMethocarbamol 500 mg/1Tablet, CoatedOralCoupler LLC67046-053867046-0538-03
MethocarbamolMethocarbamol 100 mg/mLInjectionIntramuscular, Intravenous, IntravenousJVET PHARMACEUTICALS LLC86211-11486211-0114-10

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
ProductStrengthForm · routeLabelerProduct NDC
MethocarbamolMethocarbamol 500 mg/1TabletOralProficient Rx LP82804-121
MethocarbamolMethocarbamol 500 mg/1TabletOralAsclemed USA, Inc.76420-626
MethocarbamolMethocarbamol 750 mg/1TabletOralBryant Ranch Prepack71335-2305
MethocarbamolMethocarbamol 750 mg/1TabletOralAsclemed USA, Inc.76420-638
MethocarbamolMethocarbamol 750 mg/1TabletOralAsclemed USA, Inc.76420-258
MethocarbamolMethocarbamol 500 mg/1TabletOralAsclemed USA, Inc.76420-667
MethocarbamolMethocarbamol 500 mg/1TabletOralDoc Rx69306-500
MethocarbamolMethocarbamol 500 mg/1TabletOralDoc Rx69306-510
MethocarbamolMethocarbamol 750 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0490
MethocarbamolMethocarbamol 750 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC53401-035
MethocarbamolMethocarbamol 500 mg/1TabletOralPreferred Pharmaceuticals, Inc68788-7973
MethocarbamolMethocarbamol 750 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7980
MethocarbamolMethocarbamol 500 mg/1TabletOralBryant Ranch Prepack71335-3105
MethocarbamolMethocarbamol 500 mg/1TabletOralA-S Medication Solutions50090-5907
MethocarbamolMethocarbamol 500 mg/1TabletOralDirect_rx72189-665
MethocarbamolMethocarbamol 500 mg/1TabletOralMedsource Pharmaceuticals45865-242
MethocarbamolMethocarbamol 500 mg/1TabletOralBryant Ranch Prepack71335-2383
MethocarbamolMethocarbamol 750 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-725
MethocarbamolMethocarbamol 500 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0283
MethocarbamolMethocarbamol 500 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3636

Showing 20 of 39.

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