Prescription drug · ANDA

Methocarbamol NDC 72789-041

Methocarbamol 750 mg/1 · Tablet, Film coated · Oral · PD-Rx Pharmaceuticals, Inc.

NDC codes

FDA NDC Directory
Product NDC (as listed)72789-041Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0041Add 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
72789-041-207278900412020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20)Marketed from Feb 13, 2020
72789-041-307278900413030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30)Marketed from Jan 16, 2020
72789-041-407278900414040 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40)Marketed from Jan 6, 2020
72789-041-607278900416060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)Marketed from Dec 19, 2019

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, Film coated
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208507
Marketing start
Listing expires
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 72789-041_4af347a6-c3c7-7d45-e063-6294a90a1132SPL ID 4af347a6-c3c7-7d45-e063-6294a90a1132SPL set ID 440bf1ba-a704-4c35-bece-0a0987fc0c11RxCUI 197944UNII 125OD7737XUPC 0372789041308
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

N472789004120 followed by a unit qualifier and the quantity

Package 72789-0041-20. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE 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 72789-041

What is NDC 72789-041?
72789-041 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, film coated, listed with the FDA by PD-Rx Pharmaceuticals, 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?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. 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 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
ProductStrengthForm · routeLabelerProduct NDC
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-3578
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4793
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralProficient Rx LP71205-103
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralProficient Rx LP71205-285
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0828
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0970
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-174
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-012
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-021
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-022
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-110
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralUNICHEM PHARMACEUTICALS (USA), INC.76385-123
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralUNICHEM PHARMACEUTICALS (USA), INC.76385-124
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-040
MethocarbamolMethocarbamol 500 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0138
MethocarbamolMethocarbamol 750 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0171

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