NDC codes

FDA NDC Directory
Product NDC (as listed)63868-187Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63868-0187Add 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
63868-187-2463868018724638680187241 BLISTER PACK in 1 CARTON (63868-187-24) / 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
Chain Drug Marketing AssociationNDC labeler code 63868
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 63868-187_a5353efd-016c-46bf-9b82-06b064ccf392SPL ID a5353efd-016c-46bf-9b82-06b064ccf392SPL set ID b85a042f-88ed-4961-a397-72974199c3dfRxCUI 1489932UNII J50OIX95QV, WIQ1H85SYPUPC 0635515996038

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

N463868018724 followed by a unit qualifier and the quantity

Package 63868-0187-24. 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 63868-187

What is NDC 63868-187?
63868-187 is the product NDC for Quality Choice Antibacterial Plus Urinary Pain Relief, Methenamine 162 mg/1; Sodium salicylate 162.5 mg/1 tablet, listed with the FDA by Chain Drug Marketing Association. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Quality Choice Antibacterial Plus Urinary Pain Relief (Methenamine, Sodium salicylate).
What is the active ingredient?
Methenamine, Sodium salicylate.
Who is the labeler?
Chain Drug Marketing Association, NDC labeler code 63868. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Quality Choice Antibacterial Plus Urinary Pain Relief?
1 other product NDC are listed under this name. See all Quality Choice Antibacterial Plus Urinary Pain Relief 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 Quality Choice Antibacterial Plus Urinary Pain Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Quality Choice Antibacterial Plus Urinary Pain Reliefmethenamine, sodium salicylateMethenamine 162 mg/1; Sodium salicylate 162.5 mg/1TabletOralChain Drug Marketing Association83324-19883324-0198-24

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