What is NDC 35561-211?

35561-211 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, coated, listed with the FDA by Bostal LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Bostal LLC, NDC labeler code 35561. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Methocarbamol NDC 35561-211 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)35561-211Labeler and product segments. Claims need a package NDC.

Product NDC at billing width35561-0211Add 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
35561-211-12	3556102111235561021112	100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-211-12)Marketed from Oct 9, 2018
35561-211-13	3556102111335561021113	500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-211-13)Marketed from Oct 9, 2018

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, Coated
Route: Oral
Labeler: Bostal LLCNDC labeler code 35561
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 200958
Marketing start: Oct 9, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 35561-211_49fcc548-27fe-58d0-e063-6294a90af96dSPL ID 49fcc548-27fe-58d0-e063-6294a90af96dSPL set ID d8f10211-f96e-4cf3-9b49-986eb51b703dRxCUI 197943, 197944, 2611794UNII 125OD7737XUPC 0335561212129, 0335561211122, 0335561349122, 0335561349139, 0335561211139, 0335561212136
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

N435561021112 followed by a unit qualifier and the quantity

Package 35561-0211-12. 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

Current FDA label (SPL), effective Feb 4, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Methocarbamol is 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 35561-211

What is NDC 35561-211?: 35561-211 is the product NDC for Methocarbamol, Methocarbamol 750 mg/1 tablet, coated, listed with the FDA by Bostal 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?: Bostal LLC, NDC labeler code 35561. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Methocarbamolmethocarbamol tablets	Methocarbamol 500 mg/1	Tablet, CoatedOral	American Health Packaging	60687-945	60687-0945-01
Methocarbamolmethocarbamol tablets	Methocarbamol 750 mg/1	Tablet, CoatedOral	American Health Packaging	60687-956	60687-0956-01
Methocarbamol	Methocarbamol 500 mg/1	TabletOral	REGIMED MEDICAL	25685-240	25685-0240-10
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

All 201 Methocarbamol NDCs

Other NDCs under ANDA 200958

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

FDA NDC Directory listings under ANDA 200958
Product	Strength	Form · route	Labeler	Product NDC
Methocarbamol	Methocarbamol 1000 mg/1	Tablet, CoatedOral	Misemer Pharmaceutical	0276-0510
Methocarbamol	Methocarbamol 500 mg/1	Tablet, CoatedOral	Bostal LLC	35561-212
Methocarbamol	Methocarbamol 1000 mg/1	Tablet, CoatedOral	Bostal LLC	35561-349
Methocarbamol	Methocarbamol 1000 mg/1	Tablet, CoatedOral	Trifluent Pharma LLC	73352-510
Methocarbamol	Methocarbamol 1000 mg/1	Tablet, CoatedOral	Oncora Pharma, LLC	85477-101