NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5727Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5727Add 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
50090-5727-2500905727025009057270212 TABLET in 1 BOTTLE (50090-5727-2)Marketed from Sep 28, 2021

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
A-S Medication SolutionsNDC labeler code 50090
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 50090-5727_9d0bedaa-8707-4659-b79d-f34989c2d26cSPL ID 9d0bedaa-8707-4659-b79d-f34989c2d26cSPL set ID 51c96c7a-0a38-41a5-a6c9-7f45db65fddaRxCUI 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

N450090572702 followed by a unit qualifier and the quantity

Package 50090-5727-02. 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 50090-5727

What is NDC 50090-5727?
50090-5727 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, 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?
A-S Medication Solutions, NDC labeler code 50090. 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 Solutions50090-5728
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralRedpharm Drug67296-2138
Meclizine HydrochlorideMeclizine hydrochloride 25 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3748
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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