NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3748Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3748Add 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 NDC11-digit (billing)PackageCopy
68071-3748-468071374804680713748044 TABLET in 1 BOTTLE (68071-3748-4)Marketed from May 15, 2025
68071-3748-668071374806680713748066 TABLET in 1 BOTTLE (68071-3748-6)Marketed from Dec 18, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
NuCare Pharmaceuticals, Inc.NDC labeler code 68071
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213957
Marketing start
Listing expires
Other FDA classes
Emesis Suppression (Physiologic effect)
Identifiers
Product ID 68071-3748_352f1797-e850-efb9-e063-6294a90a6442SPL ID 352f1797-e850-efb9-e063-6294a90a6442SPL set ID 2990e296-2d60-70c0-e063-6394a90abbe4RxCUI 995666UNII HDP7W44CIOUPC 0368071374865
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

N468071374804 followed by a unit qualifier and the quantity

Package 68071-3748-04. 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 .

Indications (excerpt from the label)

Meclizine hydrochloride tablets are indicated for the treatment of vertigo associated with diseases affecting the vestibular system in adults. Meclizine hydrochloride tablets are 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 68071-3748

What is NDC 68071-3748?
68071-3748 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals, 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?
NuCare Pharmaceuticals, Inc., NDC labeler code 68071. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-99760760-0997-30
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralCoupler LLC67046-086967046-0869-03
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-417068788-4170-0168788-4170-03
Meclizine HydrochloridemeclizineMeclizine hydrochloride 50 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-94323155-0943-0123155-0943-10
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-049480425-0494-0180425-0494-0280425-0494-03
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralNorthwind Health Company, LLC82868-05882868-0058-2082868-0058-30
Meclizine HydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-863368788-8633-0168788-8633-03
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-741750090-7417-0050090-7417-0150090-7417-04+1 more
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-741650090-7416-02
Meclizine HydrochloridemeclizineMeclizine hydrochloride 50 mg/1TabletOralAurobindo Pharma Limited59651-80959651-0809-0559651-0809-90

All 84 Meclizine Hydrochloride NDCs

Other NDCs under ANDA 213957

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

FDA NDC Directory listings under ANDA 213957
ProductStrengthForm · routeLabelerProduct NDC
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-5727
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-5728
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralRedpharm Drug67296-2138
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3791
Meclizine HydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.70710-1161
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.70710-1162
Meclizine HydrochlorideMeclizine hydrochloride 12.5 mg/1TabletOralZydus Lifesciences Limited70771-1539
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralZydus Lifesciences Limited70771-1540

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