What is NDC 59088-724?

59088-724 is the product NDC for Methocarb 500-EZS (methocarbamol) kit, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Methocarb 500-EZS (Methocarbamol).

PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Methocarb 500-EZS?

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.

Methocarb 500-EZS NDC 59088-724 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-724Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0724Add 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
59088-724-00	5908807240059088072400	1 KIT in 1 KIT (59088-724-00) * 100 TABLET, FILM COATED in 1 BOTTLE (69543-134-10)Marketed from Oct 23, 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): Methocarb 500-EZS
Generic name (nonproprietary): methocarbamol
Dosage form: Kit
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Oct 23, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 59088-724_b3ca019e-98e0-1007-e053-2a95a90a1690SPL ID b3ca019e-98e0-1007-e053-2a95a90a1690SPL set ID 383ce408-1085-43e7-944e-957ff2a9d553RxCUI 197943UPC 0731477272217

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N459088072400 followed by a unit qualifier and the quantity

Package 59088-0724-00. 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 Nov 10, 2020.

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 59088-724

What is NDC 59088-724?: 59088-724 is the product NDC for Methocarb 500-EZS (methocarbamol) kit, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Methocarb 500-EZS (Methocarbamol).
Who is the labeler?: PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Methocarb 500-EZS?: 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.

Methocarb 500-EZS (Methocarbamol) NDC 59088-724