What is NDC 72789-021?

72789-021 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, film coated, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 7 package NDCs, shown above in 10- and 11-digit form.

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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Methocarbamol NDC 72789-021 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72789-021Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72789-0021Add 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
72789-021-01	72789002101	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-01)Marketed from Oct 24, 2019
72789-021-60	72789002160	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-60)Marketed from Sep 12, 2023
72789-021-82	72789002182	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-82)Marketed from Oct 24, 2019
72789-021-90	72789002190	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-90)Marketed from Sep 12, 2023
72789-021-93	72789002193	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-93)Marketed from Oct 24, 2019
72789-021-94	72789002194	270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-94)Marketed from Oct 24, 2019
72789-021-99	72789002199	240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-99)Marketed from Oct 24, 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 — 500 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: Jan 15, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 72789-021_4af30668-89af-69a1-e063-6394a90a38f4SPL ID 4af30668-89af-69a1-e063-6394a90a38f4SPL set ID 943fe701-5d7d-4abe-a529-c5a548e94bc6RxCUI 197943UNII 125OD7737XUPC 0372789021010
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

N472789002101 followed by a unit qualifier and the quantity

Package 72789-0021-01. 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 Feb 16, 2026.

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 72789-021

What is NDC 72789-021?: 72789-021 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, film coated, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 7 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
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 500 mg/1	Tablet, Film coatedOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0138
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.	72789-012
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