NDC codes

FDA NDC Directory
Product NDC (as listed)17714-117Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17714-0117Add 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
17714-117-0117714011701100 TABLET in 1 BOTTLE (17714-117-01)Marketed from Jul 1, 2013

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)
Meclizine HCL 12.5 mg
Generic name (nonproprietary)
meclizine hcl 12.5 mg
Active ingredients
Meclizine hydrochloride — 12.5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Over-the-counter drug
Marketing category
OTC monograph (final)Application part336
Marketing start
Listing expires
Other FDA classes
Emesis Suppression (Physiologic effect)
Identifiers
Product ID 17714-117_5cc9755e-6d41-fa9f-e053-2991aa0afbefSPL ID 5cc9755e-6d41-fa9f-e053-2991aa0afbefSPL set ID 76efad7e-e765-430f-9232-63553d02f2c5RxCUI 995624UNII HDP7W44CIO
Pharmacologic class
Antiemetic

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

N417714011701 followed by a unit qualifier and the quantity

Package 17714-0117-01. 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 prevents and treats nausea, vomiting, or dizziness due to motion sickness for other uses, consult your doctor

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under part336

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

FDA NDC Directory listings under part336
ProductStrengthForm · routeLabelerProduct NDC
Meclizine HCL 25 mgmeclizine hclMeclizine hydrochloride 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7982
Motion Sickness Reliefmeclizine hclMeclizine hydrochloride 25 mg/1Tablet, ChewableOralPuraCap Pharmaceutical LLC51013-322
Meclizine HCLmeclizine hcl 25mg chewable tabletsMeclizine hydrochloride 25 mg/1Tablet, ChewableOralRichmond Pharmaceuticals, Inc.54738-025
Motion Sickness Reliefmeclizine hclMeclizine hydrochloride 25 mg/1Tablet, ChewableOralCVS PHARMACY, INC.69842-395
Meclizine HCLmeclizine hcl 25mg chewable tabletsMeclizine hydrochloride 25 mg/1Tablet, ChewableOralAdvance Pharmaceutical Inc.17714-115
Meclizinemeclizine hcl 25mgMeclizine hydrochloride 25 mg/1Tablet, ChewableOralBryant Ranch Prepack71335-1215
Motion-Time Chewablemeclizine hclMeclizine hydrochloride 25 mg/251Tablet, ChewableOralTime-Cap Labs, Inc49483-333

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