What is NDC 16571-661?

16571-661 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by Rising Pharma Holdings, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Rising Pharma Holdings, Inc., NDC labeler code 16571. 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 16571-661

NDC codes

FDA NDC Directory

Product NDC (as listed)16571-661Labeler and product segments. Claims need a package NDC.

Product NDC at billing width16571-0661Add 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
16571-661-01	1657106610116571066101	100 TABLET in 1 BOTTLE (16571-661-01)Marketed from Jan 15, 2020
16571-661-10	1657106611016571066110	1000 TABLET in 1 BOTTLE (16571-661-10)Marketed from Jan 15, 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: Rising Pharma Holdings, Inc.NDC labeler code 16571
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 010721
Marketing start: Jan 15, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Emesis Suppression (Physiologic effect)
Identifiers: Product ID 16571-661_2be27ea6-3d0a-4036-ab42-fea4720daa34SPL ID 2be27ea6-3d0a-4036-ab42-fea4720daa34SPL set ID c9ddc39c-bc6b-42f1-8c5f-5aff2d79c4bdRxCUI 995624, 995632, 995666, 995686UNII 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

N416571066101 followed by a unit qualifier and the quantity

Package 16571-0661-01. 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 Jun 2, 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.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 16571-661

What is NDC 16571-661?: 16571-661 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by Rising Pharma Holdings, 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?: Rising Pharma Holdings, Inc., NDC labeler code 16571. 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 NDA 010721

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

FDA NDC Directory listings under NDA 010721
Product	Strength	Form · route	Labeler	Product NDC
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Rising Pharma Holdings, Inc.	16571-660
Meclizine Hydrochloride	Meclizine hydrochloride 50 mg/1	TabletOral	Rising Pharma Holdings, Inc.	16571-662
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	Tablet, ChewableOral	Rising Pharma Holdings, Inc.	16571-663
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-661
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Coupler LLC	67046-0869
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-2380
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-2416
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8633
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-3768
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-3815
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Proficient Rx LP	71205-647
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Proficient Rx LP	71205-786
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Bryant Ranch Prepack	71335-1825
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-1872
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-3139
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Direct_Rx	72189-237
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	DirectRx	72189-302
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Asclemed USA, Inc.	76420-797
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Asclemed USA, Inc.	76420-798
Meclizine Hydrochloride	Meclizine hydrochloride 50 mg/1	TabletOral	Asclemed USA, Inc.	76420-799

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