NDC codes

FDA NDC Directory
Product NDC (as listed)0615-8514Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00615-8514Add 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
0615-8514-390061585143930 TABLET in 1 BLISTER PACK (0615-8514-39)Marketed from Jul 15, 2024

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 12.5 mg/1
Dosage form
Tablet
Route
Oral
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 0615-8514_7c702061-6604-4b46-b035-dd0fb4d25165SPL ID 7c702061-6604-4b46-b035-dd0fb4d25165SPL set ID 1a33dec1-8d59-48bd-aaef-77d162194d57RxCUI 995624, 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

N400615851439 followed by a unit qualifier and the quantity

Package 00615-8514-39. 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)

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/1TabletOralAurobindo Pharma Limited59651-808
Meclizine HydrochloridemeclizineMeclizine hydrochloride 12.5 mg/1TabletOralAurobindo Pharma Limited59651-807
Meclizine HydrochloridemeclizineMeclizine hydrochloride 50 mg/1TabletOralAurobindo Pharma Limited59651-809
Meclizine HydrochloridemeclizineMeclizine hydrochloride 12.5 mg/1TabletOralBryant Ranch Prepack71335-3141
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-7417
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralBryant Ranch Prepack71335-3157
Meclizine HydrochloridemeclizineMeclizine hydrochloride 25 mg/1TabletOralA-S Medication Solutions50090-7416
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 12.5 mg/1TabletOralRedpharm Drug67296-2250

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