NDC codes

FDA NDC Directory
Product NDC (as listed)71335-3141Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-3141Add 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
71335-3141-1713353141017133531410130 TABLET in 1 BOTTLE (71335-3141-1)Marketed from Jun 8, 2026
71335-3141-2713353141027133531410260 TABLET in 1 BOTTLE (71335-3141-2)Marketed from Jun 8, 2026
71335-3141-3713353141037133531410390 TABLET in 1 BOTTLE (71335-3141-3)Marketed from Jun 8, 2026
71335-3141-4713353141047133531410428 TABLET in 1 BOTTLE (71335-3141-4)Marketed from Jun 8, 2026
71335-3141-5713353141057133531410520 TABLET in 1 BOTTLE (71335-3141-5)Marketed from Jun 8, 2026
71335-3141-67133531410671335314106120 TABLET in 1 BOTTLE (71335-3141-6)Marketed from Jun 8, 2026
71335-3141-77133531410771335314107100 TABLET in 1 BOTTLE (71335-3141-7)Marketed from Jun 8, 2026
71335-3141-8713353141087133531410810 TABLET in 1 BOTTLE (71335-3141-8)Marketed from Jun 8, 2026

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
Active ingredients
Meclizine hydrochloride — 12.5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202640
Marketing start
Listing expires
Other FDA classes
Emesis Suppression (Physiologic effect)
Identifiers
Product ID 71335-3141_6c523373-60b5-436e-8e78-10e9bb9c997aSPL ID 6c523373-60b5-436e-8e78-10e9bb9c997aSPL set ID 1079db3f-d8ad-4c25-aa91-8ac8054ee4f2RxCUI 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

N471335314101 followed by a unit qualifier and the quantity

Package 71335-3141-01. 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 .

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 71335-3141

What is NDC 71335-3141?
71335-3141 is the product NDC for Meclizine Hydrochloride (meclizine), Meclizine hydrochloride 12.5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Meclizine Hydrochloride (Meclizine).
What is the active ingredient?
Meclizine hydrochloride.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. 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 202640

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

FDA NDC Directory listings under ANDA 202640
ProductStrengthForm · routeLabelerProduct NDC
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4170
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-7417
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-7416
Meclizine HydrochloridemeclizineMeclizine hydrochloride 50 mg/1TabletOralAurobindo Pharma Limited59651-809
Meclizine HydrochloridemeclizineMeclizine hydrochloride 12.5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8514
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8515
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralRedpharm Drug67296-2205
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralAurobindo Pharma Limited59651-808
Meclizine HydrochloridemeclizineMeclizine hydrochloride 12.5 mg/1TabletOralAurobindo Pharma Limited59651-807
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralBryant Ranch Prepack71335-3157
Meclizine HydrochloridemeclizineMeclizine hydrochloride 12.5 mg/1TabletOralRedpharm Drug67296-2250
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-997

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