What is NDC 72162-1690?

72162-1690 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 12.5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Meclizine Hydrochloride?

83 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Meclizine Hydrochloride NDC 72162-1690

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 NDC	11-digit (billing)	Package	Copy
72162-1690-0	7216216900072162169000	1000 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
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040659
Marketing start: Jun 4, 2010
Marketing end: Oct 31, 2026
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 Oct 31, 2025.

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)

About NDC 72162-1690

What is NDC 72162-1690?: 72162-1690 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 12.5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Meclizine Hydrochloride.
What is the active ingredient?: Meclizine hydrochloride.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Meclizine Hydrochloride?: 83 other product NDCs are listed under this name. See all Meclizine Hydrochloride 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 Meclizine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 25 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-997	60760-0997-30
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Coupler LLC	67046-0869	67046-0869-03
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4170	68788-4170-0168788-4170-03
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 50 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-943	23155-0943-0123155-0943-10
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0494	80425-0494-0180425-0494-0280425-0494-03
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Northwind Health Company, LLC	82868-058	82868-0058-2082868-0058-30
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8633	68788-8633-0168788-8633-03
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-7417	50090-7417-0050090-7417-0150090-7417-04+1 more
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-7416	50090-7416-02
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 50 mg/1	TabletOral	Aurobindo Pharma Limited	59651-809	59651-0809-0559651-0809-90

All 84 Meclizine Hydrochloride NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Northwind Health Company, LLC	51655-107
Meclizine Hydrochloridemeclizine hydrocloride	Meclizine hydrochloride 25 mg/1	TabletOral	Jubilant Cadista Pharmacuticals Inc.	59746-121
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Jubilant Cadista Pharmacuticals Inc.	59746-122
Meclizine Hydrochloridemeclizine hydrocloride	Meclizine hydrochloride 25 mg/1	TabletOral	Proficient Rx LP	63187-996
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Bryant Ranch Prepack	63629-2432
Meclizine Hydrochloridemeclizine hydrocloride	Meclizine hydrochloride 25 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3017
Meclizine Hydrochloridemeclizine hydrocloride	Meclizine hydrochloride 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-1308
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Proficient Rx LP	71205-416
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0153
Meclizine Hydrochloridemeclizine hydrocloride	Meclizine hydrochloride 25 mg/1	TabletOral	Bryant Ranch Prepack	71335-0503
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-1563
Meclizine Hydrochloridemeclizine hydrocloride	Meclizine hydrochloride 25 mg/1	TabletOral	Asclemed USA, Inc.	76420-130
Meclizine Hydrocloride	Meclizine hydrochloride 25 mg/1	TabletOral	QPharma Inc	42708-102