What is NDC 70771-1539?

70771-1539 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 12.5 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 5 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 70771. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Meclizine Hydrochloride NDC 70771-1539

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1539Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1539Add 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 NDC	11-digit (billing)	Package
70771-1539-0	7077115390070771153900	1000 TABLET in 1 BOTTLE (70771-1539-0)Marketed from Oct 29, 2020
70771-1539-1	7077115390170771153901	100 TABLET in 1 BOTTLE (70771-1539-1)Marketed from Oct 29, 2020
70771-1539-3	7077115390370771153903	30 TABLET in 1 BOTTLE (70771-1539-3)Marketed from Oct 29, 2020
70771-1539-4	7077115390470771153904	10 BLISTER PACK in 1 CARTON (70771-1539-4) / 10 TABLET in 1 BLISTER PACK (70771-1539-2)Marketed from Oct 29, 2020
70771-1539-9	7077115390970771153909	90 TABLET in 1 BOTTLE (70771-1539-9)Marketed from Oct 29, 2020

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 — 12.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213957
Marketing start: Oct 29, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Emesis Suppression (Physiologic effect)
Identifiers: Product ID 70771-1539_83635604-72b7-4eb4-b8d9-5ae556041b4dSPL ID 83635604-72b7-4eb4-b8d9-5ae556041b4dSPL set ID cf157a71-f80a-4fb7-b892-7102b65a8ec0RxCUI 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

N470771153900 followed by a unit qualifier and the quantity

Package 70771-1539-00. 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 Aug 28, 2023.

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 70771-1539

What is NDC 70771-1539?: 70771-1539 is the product NDC for Meclizine Hydrochloride, Meclizine hydrochloride 12.5 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 5 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?: Zydus Lifesciences Limited, NDC labeler code 70771. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 25 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-997	60760-0997-30
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Coupler LLC	67046-0869	67046-0869-03
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4170	68788-4170-0168788-4170-03
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 50 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-943	23155-0943-0123155-0943-10
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0494	80425-0494-0180425-0494-0280425-0494-03
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Northwind Health Company, LLC	82868-058	82868-0058-2082868-0058-30
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8633	68788-8633-0168788-8633-03
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-7417	50090-7417-0050090-7417-0150090-7417-04+1 more
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-7416	50090-7416-02
Meclizine Hydrochloridemeclizine	Meclizine hydrochloride 50 mg/1	TabletOral	Aurobindo Pharma Limited	59651-809	59651-0809-0559651-0809-90

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
Product	Strength	Form · route	Labeler	Product NDC
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-5727
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	A-S Medication Solutions	50090-5728
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Redpharm Drug	67296-2138
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3748
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3791
Meclizine Hydrochloride	Meclizine hydrochloride 12.5 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-1161
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Zydus Pharmaceuticals (USA) Inc.	70710-1162
Meclizine Hydrochloride	Meclizine hydrochloride 25 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1540