What is NDC 72245-873?

72245-873 is the product NDC for Tanlor (methocarbamol), Methocarbamol 1000 mg/1 tablet, film coated, listed with the FDA by Forte Bio-Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.

Forte Bio-Pharma, NDC labeler code 72245. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Tanlor?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Tanlor NDC 72245-873 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72245-873Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72245-0873Add 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
72245-873-10	7224508731072245087310	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72245-873-10)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): Tanlor
Generic name (nonproprietary): methocarbamol
Active ingredients: Methocarbamol — 1000 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Forte Bio-PharmaNDC labeler code 72245
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 72245-873_1dd5eca2-4ad3-5c03-e063-6394a90aa9b0SPL ID 1dd5eca2-4ad3-5c03-e063-6394a90aa9b0SPL set ID 1dd5f7fd-7b3b-8669-e063-6394a90abe95RxCUI 2611794, 2691000UNII 125OD7737XUPC 0372245873108
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

N472245087310 followed by a unit qualifier and the quantity

Package 72245-0873-10. 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 Jul 22, 2024.

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 72245-873

What is NDC 72245-873?: 72245-873 is the product NDC for Tanlor (methocarbamol), Methocarbamol 1000 mg/1 tablet, film coated, listed with the FDA by Forte Bio-Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Tanlor (Methocarbamol).
What is the active ingredient?: Methocarbamol.
Who is the labeler?: Forte Bio-Pharma, NDC labeler code 72245. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Tanlor?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

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
methocarbamol	Methocarbamol 1000 mg/1	Tablet, Film coatedOral	FH2 PHARMA LLC	72887-873

Tanlor (Methocarbamol) NDC 72245-873