NDC codes

FDA NDC Directory
Product NDC (as listed)71335-9751Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-9751Add 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
71335-9751-071335975100120 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-0)Marketed from Dec 12, 2024
71335-9751-17133597510130 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-1)Marketed from Sep 5, 2023
71335-9751-27133597510220 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-2)Marketed from Aug 10, 2023
71335-9751-37133597510325 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-3)Marketed from Dec 12, 2024
71335-9751-47133597510440 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-4)Marketed from Dec 12, 2024
71335-9751-57133597510560 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-5)Marketed from Dec 12, 2024
71335-9751-67133597510690 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-6)Marketed from Jun 19, 2024
71335-9751-7713359751078 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-7)Marketed from Dec 12, 2024
71335-9751-87133597510814 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-8)Marketed from Aug 21, 2024
71335-9751-97133597510910 TABLET, CHEWABLE in 1 BOTTLE (71335-9751-9)Marketed from Aug 7, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Generic name (nonproprietary)
meclizine hydrochloride chewable
Active ingredients
Meclizine hydrochloride — 25 mg/1
Dosage form
Tablet, Chewable
Route
Oral
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M009.50
Marketing start
Listing expires
Other FDA classes
Emesis Suppression (Physiologic effect)
Identifiers
Product ID 71335-9751_b5813836-d2ea-4aea-b894-fe428dd7e91dSPL ID b5813836-d2ea-4aea-b894-fe428dd7e91dSPL set ID 12446adb-0ff6-4f92-8bb2-b64b11d47e76RxCUI 995632UNII 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

N471335975100 followed by a unit qualifier and the quantity

Package 71335-9751-00. 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 .

Indications (excerpt from the label)

Uses prevents and treats nausea, vomiting or dizziness due to motion sickness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under M009.50

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

FDA NDC Directory listings under M009.50
ProductStrengthForm · routeLabelerProduct NDC
Meclizine HClmeclizine hydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralRising Pharma Holdings, Inc.57237-333
Meclizine HClmeclizine hydrochloride chewableMeclizine hydrochloride 25 mg/1Tablet, ChewableOralRising Pharma Holdings, Inc.16571-824
Diphenhydramine Oral Liquiddiphenhydramine hydrochlorideDiphenhydramine hydrochloride 12.5 mg/5mLLiquidOralRising Pharma Holdings, Inc.57237-305
Diphenhydramine HCl Oral Solutiondiphenhydramine hcl oralDiphenhydramine hydrochloride 12.5 mg/5mLSolutionOralRising Pharma Holdings, Inc.57237-317
Diphenhydramine HCl Oral Solutiondiphenhydramine hcl oralDiphenhydramine hydrochloride 25 mg/10mLSolutionOralRising Pharma Holdings, Inc.57237-318

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