NDC codes

FDA NDC Directory
Product NDC (as listed)60760-997Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60760-0997Add 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
60760-997-30607600997306076009973030 TABLET in 1 BOTTLE, PLASTIC (60760-997-30)Marketed from Oct 6, 2026

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
Active ingredients
Meclizine hydrochloride — 25 mg/1
Dosage form
Tablet
Route
Oral
Labeler
St. Mary's Medical Park PharmacyNDC labeler code 60760
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 60760-997_5d2ff6a3-7bfc-746c-e063-6394a90a319fSPL ID 5d2ff6a3-7bfc-746c-e063-6394a90a319f
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

N460760099730 followed by a unit qualifier and the quantity

Package 60760-0997-30. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 60760-997

What is NDC 60760-997?
60760-997 is the product NDC for Meclizine Hydrochloride (meclizine), Meclizine hydrochloride 25 mg/1 tablet, listed with the FDA by St. Mary's Medical Park Pharmacy. It has 1 package NDC, 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?
St. Mary's Medical Park Pharmacy, NDC labeler code 60760. 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?
90 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 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 12.5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-851400615-8514-39
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-851500615-8515-39
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-741650090-7416-02
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-741750090-7417-0050090-7417-0150090-7417-04+1 more

All 91 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 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/1TabletOralA-S Medication Solutions50090-7416
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-7417
Meclizine HydrochloridemeclizineMeclizine hydrochloride 12.5 mg/1TabletOralAurobindo Pharma Limited59651-807
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralAurobindo Pharma Limited59651-808
Meclizine HydrochloridemeclizineMeclizine hydrochloride 50 mg/1TabletOralAurobindo Pharma Limited59651-809
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralRedpharm Drug67296-2205
Meclizine HydrochloridemeclizineMeclizine hydrochloride 12.5 mg/1TabletOralRedpharm Drug67296-2250
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4170
Meclizine HydrochloridemeclizineMeclizine hydrochloride 12.5 mg/1TabletOralBryant Ranch Prepack71335-3141
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralBryant Ranch Prepack71335-3157

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