Excluded / Inactive
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for Meclizine HCl 12.5 mg Oral Tablet (RxCUI 995624). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.
Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.
Manufacturer Quick Index
Found 72 manufactured products
A-S Medication Solutions
NDC Product
Meclizine Hydrochloride NDC 50090-5203
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
APNAR PHARMA LP
NDC Product
Human Otc DrugMeclizine Hydrochloride NDC 24689-138
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
NDC Product
Human Otc DrugMeclizine Hydrochloride NDC 24689-139
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Advance Pharmaceutical Inc.
NDC Product
Human Otc DrugMeclizine Hcl 12.5 Mg NDC 17714-117
- Generic Name
- Meclizine Hcl 12.5 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH FINAL
Active Listing
Advanced Rx LLC
NDC Product
Human Otc DrugMeclizine NDC 80513-427
- Generic Name
- Meclizine Hcl 12.5 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Aidarex Pharmaceuticals LLC
NDC Product
Meclizine Hcl NDC 33261-748
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Excluded / Inactive
American Health Packaging
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 60687-730
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 60687-775
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals LLC
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 65162-441
- Generic Name
- Meclizine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 65162-442
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 65162-444
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals of New York LLC
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 53746-441
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 53746-442
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Asclemed USA, Inc.
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 76420-797
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 76420-798
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 76420-799
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 59651-807
- Generic Name
- Meclizine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 59651-808
- Generic Name
- Meclizine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 59651-809
- Generic Name
- Meclizine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
AvPAK
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 50268-522
- Generic Name
- Meclizine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 50268-523
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Blenheim Pharmacal, Inc.
NDC Product
Meclizine Hcl NDC 10544-249
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Excluded / Inactive
BluePoint Laboratories
NDC Product
Human Otc DrugMeclizine Hcl NDC 68001-528
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 63629-2432
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 71335-0153
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 71335-1563
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 71335-1872
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 72162-1690
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Chartwell RX, LLC
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 62135-952
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 62135-953
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 62135-954
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
DIRECT RX
NDC Product
Meclizine NDC 61919-301
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
DirectRx
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 72189-302
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Direct_Rx
NDC Product
Meclizine Hydrochloride NDC 61919-886
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Epic Pharma LLC
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 42806-012
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 42806-014
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
H.J. Harkins Company, Inc.
NDC Product
Meclizine Hydrochloride NDC 52959-225
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Jubilant Cadista Pharmacuticals Inc.
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 59746-121
- Generic Name
- Meclizine Hydrocloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 59746-122
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Major Pharmaceuticals
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 0904-7375
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 0904-7376
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NCS HealthCare of KY, LLC dba Vangard Labs
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 0615-8514
- Generic Name
- Meclizine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 0615-8515
- Generic Name
- Meclizine
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Pharbest Pharmaceuticals, Inc.
NDC Product
Human Otc DrugMeclizine NDC 16103-386
- Generic Name
- Meclizine Hcl 12.5 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Physicians Total Care, Inc.
NDC Product
Meclizine Hydrochloride NDC 54868-0077
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Meclizine Hydrochloride NDC 54868-0089
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 68788-8633
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 71205-416
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 71205-647
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Otc DrugMeclizine Hcl 12.5 Mg NDC 71205-762
- Generic Name
- Meclizine Hcl 12.5 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
REMEDYREPACK INC.
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 70518-3768
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
RPK Pharmaceuticals, Inc.
NDC Product
Meclizine Hydrochloride NDC 53002-6062
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
RUGBY LABORATORIES
NDC Product
Human Otc DrugMeclizine NDC 0536-1297
- Generic Name
- Meclizine Hcl 12.5 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rebel Distributors Corp.
NDC Product
Meclizine Hydrochloride NDC 21695-237
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Meclizine Hydrochloride NDC 21695-383
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
RedPharm Drug, Inc.
NDC Product
Rugby NDC 67296-1252
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Excluded / Inactive
Reliable 1 Laboratories LLC
NDC Product
Human Otc DrugMeclizine Hcl 12.5 Mg NDC 69618-027
- Generic Name
- Meclizine Hcl 12.5 Mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Rising Pharma Holdings, Inc.
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 16571-660
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 16571-661
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 16571-662
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 16571-663
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Otc DrugMeclizine Hcl NDC 57237-333
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
SDA Laboratories, Inc.
NDC Product
Meclizine NDC 66424-386
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Excluded / Inactive
STAT Rx USA LLC
NDC Product
Meclizine Hydrochloride NDC 16590-146
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Meclizine Hydrochloride NDC 16590-301
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Trigen Laboratories, Inc.
NDC Product
Meclizine Hcl NDC 13811-646
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH FINAL
Excluded / Inactive
Ulai Health LLC
NDC Product
Human Otc DrugMeclizine NDC 73057-386
- Generic Name
- Meclizine Hcl 12.5mg
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- OTC MONOGRAPH DRUG
Active Listing
Zydus Lifesciences Limited
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 70771-1539
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 70771-1540
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Zydus Pharmaceuticals (USA) Inc.
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 70710-1161
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugMeclizine Hydrochloride NDC 70710-1162
- Generic Name
- Meclizine Hydrochloride
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing