What is NDC 69842-857?

69842-857 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by CVS Pharmacy, Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

CVS Pharmacy, Inc, NDC labeler code 69842. 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 69842-857

NDC codes

FDA NDC Directory

Product NDC (as listed)69842-857Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69842-0857Add 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
69842-857-05	6984208570569842085705	2 BLISTER PACK in 1 CARTON (69842-857-05) / 8 TABLET in 1 BLISTER PACKMarketed from Oct 28, 2020
69842-857-09	6984208570969842085709	1 VIAL in 1 CARTON (69842-857-09) / 8 TABLET in 1 VIALMarketed from Aug 13, 2020

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 Hydrochloride
Generic name (nonproprietary): meclizine hydrochloride
Active ingredients: Meclizine hydrochloride — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: CVS Pharmacy, IncNDC labeler code 69842
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 009
Marketing start: Aug 13, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Emesis Suppression (Physiologic effect)
Identifiers: Product ID 69842-857_41499ece-5964-999d-e063-6394a90ab8fbSPL ID 41499ece-5964-999d-e063-6394a90ab8fbSPL set ID b57fc6c2-fbfc-24c3-e053-2995a90a3389RxCUI 995666UNII 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

N469842085705 followed by a unit qualifier and the quantity

Package 69842-0857-05. 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 16, 2025.

Indications (excerpt from the label)

Uses for prevention and treatment of these symptoms associated with motion sickness: ■ nausea ■ vomiting ■ dizziness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69842-857

What is NDC 69842-857?: 69842-857 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by CVS Pharmacy, Inc. It has 2 package NDCs, 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?: CVS Pharmacy, Inc, NDC labeler code 69842. 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 M 009

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

FDA NDC Directory listings under M 009
Product	Strength	Form · route	Labeler	Product NDC
Airmit Acedimenhydrinate	Dimenhydrinate 25 mg/1	TabletOral	Sato Pharmaceutical Co., Ltd.	49873-802
Allergy DyeFree	Diphenhydramine hydrochloride 25 mg/1	Capsule, Liquid filledOral	Allegiant Health	69168-409
Bangbrek Bee Venom Wart Corn Callus Removersalicylic acid 17%	Salicylic acid 17 mg/mL	LiquidTopical	Brilliance Trade LLC	85792-001
Boninemeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	WellSpring Pharmaceutical Corporation	65197-275
Boninemeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	WellSpring Pharmaceutical Corporation	65197-296
Boninemeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	WellSpring Pharmaceutical Corporation	65197-297
Bonine Maxmeclizine hydrochloride	Meclizine hydrochloride 50 mg/1	Tablet, ChewableOral	WellSpring Pharmaceutical Corporation	65197-520
Childrens Allergydiphenhydramine hydrochloride	Diphenhydramine hydrochloride 12.5 mg/5mL	LiquidOral	DeMoulas Market Basket	53942-505
CVS Motion Sickness Fast Meltingmeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, Orally disintegratingOral	CVS Pharmacy, Inc.	59779-534
Dimenhydrinate	Dimenhydrinate 50 mg/1	TabletOral	Major Pharmaceuticals	0904-6772
Dimenhydrinate	Dimenhydrinate 50 mg/1	TabletOral	CVS Pharmacy, Inc.	69842-206
Dimenhydrinate	Dimenhydrinate 50 mg/1	TabletOral	LEADER/ Cardinal Health 110, Inc.	70000-0404
Dramaminemeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	Medtech Products Inc.	63029-906
Dramaminemeclizine hydrochloride	Meclizine dihydrochloride 50 mg/1	PowderOral	Medtech Products Inc.	63029-912
Dramaminemeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	Medtech Products Inc.	63029-913
Dramaminemeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	Medtech Products Inc.	63029-914
Dramaminedimenhydrinate	Dimenhydrinate 50 mg/1	Tablet, ChewableOral	Lil' Drug Store Products, Inc.	66715-9809
Dramamine - Nmeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Medtech Products Inc.	63029-905
Dramamine Chewable Orangemeclizine hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	Medtech Products Inc.	63029-915
Dramamine for Kidsdimenhydrinate	Dimenhydrinate 25 mg/1	Tablet, ChewableOral	Medtech Products Inc.	63029-904

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