NDC codes

FDA NDC Directory
Product NDC (as listed)41250-557Labeler and product segments. Claims need a package NDC.
Product NDC at billing width41250-0557Add 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 NDC11-digit (billing)PackageCopy
41250-557-2441250055724412500557241 BLISTER PACK in 1 CARTON (41250-557-24) / 24 TABLET in 1 BLISTER PACKMarketed from Feb 22, 2017

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

Generic name (nonproprietary)
methenamine, sodium salicylate
Active ingredients
Methenamine — 162 mg/1Sodium salicylate — 162.5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Meijer Distribution Inc.NDC labeler code 41250
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 41250-557_06ba68f7-27f0-4e27-9216-2b1e620febeaSPL ID 06ba68f7-27f0-4e27-9216-2b1e620febeaSPL set ID 9eaaf197-9e96-4220-b49d-2f743b443623RxCUI 1489932UNII J50OIX95QV, WIQ1H85SYP

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

N441250055724 followed by a unit qualifier and the quantity

Package 41250-0557-24. 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 .

Indications (excerpt from the label)

Uses Temporarily relieves: pain & burning • frequency and urgency of urination

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 41250-557

What is NDC 41250-557?
41250-557 is the product NDC for Meijer Antibacterial Plus Urinary Pain Relief, Methenamine 162 mg/1; Sodium salicylate 162.5 mg/1 tablet, listed with the FDA by Meijer Distribution Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Meijer Antibacterial Plus Urinary Pain Relief (Methenamine, Sodium salicylate).
What is the active ingredient?
Methenamine, Sodium salicylate.
Who is the labeler?
Meijer Distribution Inc., NDC labeler code 41250. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Meijer Antibacterial Plus Urinary Pain Relief?
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.

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