What is NDC 17714-117?

17714-117 is the product NDC for Meclizine HCL 12.5 mg, Meclizine hydrochloride 12.5 mg/1 tablet, listed with the FDA by Advance Pharmaceutical Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Advance Pharmaceutical Inc., NDC labeler code 17714. 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 HCL 12.5 mg?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Meclizine HCL 12.5 mg NDC 17714-117

NDC codes

FDA NDC Directory

Product NDC (as listed)17714-117Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17714-0117Add 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
17714-117-01	1771401170117714011701	100 TABLET in 1 BOTTLE (17714-117-01)Marketed from Jul 1, 2013

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 HCL 12.5 mg
Generic name (nonproprietary): meclizine hcl 12.5 mg
Active ingredients: Meclizine hydrochloride — 12.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Advance Pharmaceutical Inc.NDC labeler code 17714
Product type: Over-the-counter drug
Marketing category: OTC monograph (final)Application part336
Marketing start: Jul 1, 2013
Listing expires: Dec 31, 2026
Other FDA classes: Emesis Suppression (Physiologic effect)
Identifiers: Product ID 17714-117_5cc9755e-6d41-fa9f-e053-2991aa0afbefSPL ID 5cc9755e-6d41-fa9f-e053-2991aa0afbefSPL set ID 76efad7e-e765-430f-9232-63553d02f2c5RxCUI 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

N417714011701 followed by a unit qualifier and the quantity

Package 17714-0117-01. 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 30, 2017.

Indications (excerpt from the label)

Uses prevents and treats nausea, vomiting, or dizziness due to motion sickness for other uses, consult your doctor

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17714-117

What is NDC 17714-117?: 17714-117 is the product NDC for Meclizine HCL 12.5 mg, Meclizine hydrochloride 12.5 mg/1 tablet, listed with the FDA by Advance Pharmaceutical Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Meclizine HCL 12.5 mg.
What is the active ingredient?: Meclizine hydrochloride.
Who is the labeler?: Advance Pharmaceutical Inc., NDC labeler code 17714. 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 HCL 12.5 mg?: 2 other product NDCs are listed under this name. See all Meclizine HCL 12.5 mg 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 HCL 12.5 mg NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Meclizine HCL 12.5 mg	Meclizine hydrochloride 12.5 mg/1	TabletOral	Reliable 1 Laboratories LLC	69618-027	69618-0027-0169618-0027-10
Meclizine HCL 12.5 mg	Meclizine hydrochloride 12.5 mg/1	TabletOral	Proficient Rx LP	71205-762	71205-0762-1071205-0762-3071205-0762-60+1 more

Other NDCs under part336

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

FDA NDC Directory listings under part336
Product	Strength	Form · route	Labeler	Product NDC
Meclizinemeclizine hcl 25mg	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	Bryant Ranch Prepack	71335-1215
Meclizine HCLmeclizine hcl 25mg chewable tablets	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	Advance Pharmaceutical Inc.	17714-115
Meclizine HCLmeclizine hcl 25mg chewable tablets	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	Richmond Pharmaceuticals, Inc.	54738-025
Meclizine HCL 25 mgmeclizine hcl	Meclizine hydrochloride 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7982
Motion Sickness Reliefmeclizine hcl	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	PuraCap Pharmaceutical LLC	51013-322
Motion Sickness Reliefmeclizine hcl	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	CVS PHARMACY, INC.	69842-395
Motion-Time Chewablemeclizine hcl	Meclizine hydrochloride 25 mg/251	Tablet, ChewableOral	Time-Cap Labs, Inc	49483-333