What is NDC 63187-258?

63187-258 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 5 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 63187. 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 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	6318702581063187025810	10 TABLET in 1 BOTTLE (63187-258-10)Marketed from Jan 1, 2019
63187-258-20	6318702582063187025820	20 TABLET in 1 BOTTLE (63187-258-20)Marketed from Jan 1, 2019
63187-258-30	6318702583063187025830	30 TABLET in 1 BOTTLE (63187-258-30)Marketed from Jan 1, 2019
63187-258-60	6318702586063187025860	60 TABLET in 1 BOTTLE (63187-258-60)Marketed from Jan 1, 2019
63187-258-90	6318702589063187025890	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 LPNDC labeler code 63187
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 200294
Marketing start: Apr 30, 2012
Listing expires: Dec 31, 2027
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)

About NDC 63187-258

What is NDC 63187-258?: 63187-258 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 5 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?: Proficient Rx LP, NDC labeler code 63187. 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 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