Meclizine Hydrochloride NDC 63187-258

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-258Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0258Add 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
63187-258-10	63187025810	10 TABLET in 1 BOTTLE (63187-258-10)Marketed from Jan 1, 2019
63187-258-20	63187025820	20 TABLET in 1 BOTTLE (63187-258-20)Marketed from Jan 1, 2019
63187-258-30	63187025830	30 TABLET in 1 BOTTLE (63187-258-30)Marketed from Jan 1, 2019
63187-258-60	63187025860	60 TABLET in 1 BOTTLE (63187-258-60)Marketed from Jan 1, 2019
63187-258-90	63187025890	90 TABLET in 1 BOTTLE (63187-258-90)Marketed from Jan 1, 2019

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: Proficient Rx LP
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 200294
Marketing start: Apr 30, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Emesis Suppression (Physiologic effect)
Identifiers: Product ID 63187-258_9a01be91-ff05-4f46-92d4-68b2d1db251cSPL ID 9a01be91-ff05-4f46-92d4-68b2d1db251cSPL set ID 91b1fd1a-1da2-4aae-826f-7de0bfe62161RxCUI 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

N463187025810 followed by a unit qualifier and the quantity

Package 63187-0258-10. 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 Jan 1, 2021. This label includes a boxed warning.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 200294

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

FDA NDC Directory listings under ANDA 200294
Product	Strength	Form · route	Labeler	Product NDC
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Epic Pharma LLC	42806-012
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Epic Pharma LLC	42806-014