NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1690Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1690Add 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
72162-1690-0721621690001000 TABLET in 1 BOTTLE (72162-1690-0)Marketed from Sep 12, 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 Hydrochloride
Generic name (nonproprietary)
meclizine hydrochloride
Active ingredients
Meclizine hydrochloride — 12.5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040659
Marketing start
Marketing end
Other FDA classes
Emesis Suppression (Physiologic effect)
Identifiers
Product ID 72162-1690_42780752-9cd6-95e5-e063-6394a90abc0fSPL ID 42780752-9cd6-95e5-e063-6394a90abc0fSPL set ID 522b55a2-313c-45e8-b1be-07746ada5b0aRxCUI 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

N472162169000 followed by a unit qualifier and the quantity

Package 72162-1690-00. 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)

Meclizine hydrochloride is indicated for the treatment of vertigo associated with diseases affecting the vestibular system in adults. Meclizine hydrochloride is indicated for the treatment of vertigo associated with diseases affecting the vestibular system in adults ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040659

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

FDA NDC Directory listings under ANDA 040659
ProductStrengthForm · routeLabelerProduct NDC
Meclizine HydroclorideMeclizine hydrochloride 25 mg/1TabletOralQPharma Inc42708-102
Meclizine Hydrochloridemeclizine hydroclorideMeclizine hydrochloride 25 mg/1TabletOralProficient Rx LP63187-996
Meclizine Hydrochloridemeclizine hydroclorideMeclizine hydrochloride 25 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3017
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralNorthwind Health Company, LLC51655-107
Meclizine Hydrochloridemeclizine hydroclorideMeclizine hydrochloride 25 mg/1TabletOralJubilant Cadista Pharmacuticals Inc.59746-121
Meclizine HydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralJubilant Cadista Pharmacuticals Inc.59746-122
Meclizine HydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralProficient Rx LP71205-416
Meclizine Hydrochloridemeclizine hydroclorideMeclizine hydrochloride 25 mg/1TabletOralBryant Ranch Prepack71335-0503
Meclizine Hydrochloridemeclizine hydroclorideMeclizine hydrochloride 25 mg/1TabletOralREMEDYREPACK INC.70518-1308
Meclizine HydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralBryant Ranch Prepack71335-1563
Meclizine HydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralBryant Ranch Prepack63629-2432
Meclizine Hydrochloridemeclizine hydroclorideMeclizine hydrochloride 25 mg/1TabletOralAsclemed USA, Inc.76420-130
Meclizine HydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralBryant Ranch Prepack71335-0153

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