What is NDC 42708-102?

42708-102 is the product NDC for Meclizine Hydrocloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by QPharma Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

QPharma Inc, NDC labeler code 42708. 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 Hydrocloride?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Meclizine Hydrocloride NDC 42708-102

NDC codes

FDA NDC Directory

Product NDC (as listed)42708-102Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42708-0102Add 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
42708-102-30	4270801023042708010230	30 TABLET in 1 BOTTLE (42708-102-30)Marketed from Oct 18, 2019 · Sample package

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 Hydrocloride
Generic name (nonproprietary): meclizine hydrocloride
Active ingredients: Meclizine hydrochloride — 25 mg/1
Dosage form: Tablet
Route: Oral
Labeler: QPharma IncNDC labeler code 42708
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 42708-102_459c95f7-ca90-7ded-e063-6394a90a0530SPL ID 459c95f7-ca90-7ded-e063-6394a90a0530SPL set ID aa0fb895-a867-4482-9bc2-16eee8bfaaa0RxCUI 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

N442708010230 followed by a unit qualifier and the quantity

Package 42708-0102-30. 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 Dec 4, 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 42708-102

What is NDC 42708-102?: 42708-102 is the product NDC for Meclizine Hydrocloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by QPharma Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Meclizine Hydrocloride.
What is the active ingredient?: Meclizine hydrochloride.
Who is the labeler?: QPharma Inc, NDC labeler code 42708. 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 Hydrocloride?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

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 Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Bryant Ranch Prepack	72162-1690
Meclizine Hydrochloridemeclizine hydrocloride	Meclizine hydrochloride 25 mg/1	TabletOral	Asclemed USA, Inc.	76420-130