What is NDC 72887-873?

72887-873 is the product NDC for methocarbamol, Methocarbamol 1000 mg/1 tablet, film coated, listed with the FDA by FH2 PHARMA LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

FH2 PHARMA LLC, NDC labeler code 72887. 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 72887-873 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72887-873Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72887-0873Add 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	Copy
72887-873-03	72887087303	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72887-873-03)Marketed from Aug 30, 2024

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 — 1000 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: FH2 PHARMA LLCNDC labeler code 72887
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212707
Marketing start: Aug 30, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 72887-873_2d7ed9b4-3cba-fb22-e063-6294a90af27aSPL ID 2d7ed9b4-3cba-fb22-e063-6294a90af27aSPL set ID 1dd56e3d-7ca7-1443-e063-6294a90a13c5RxCUI 2611794UNII 125OD7737XUPC 0372887873030
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

N472887087303 followed by a unit qualifier and the quantity

Package 72887-0873-03. 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 6, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Methocarbamol tablets 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 72887-873

What is NDC 72887-873?: 72887-873 is the product NDC for methocarbamol, Methocarbamol 1000 mg/1 tablet, film coated, listed with the FDA by FH2 PHARMA LLC. 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?: FH2 PHARMA LLC, NDC labeler code 72887. 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 212707

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

FDA NDC Directory listings under ANDA 212707
Product	Strength	Form · route	Labeler	Product NDC
Tanlormethocarbamol	Methocarbamol 1000 mg/1	Tablet, Film coatedOral	Forte Bio-Pharma	72245-873