NDC 71335-0503

MECLIZINE HYDROCHLORIDE

Meclizine Hydrocloride

MECLIZINE HYDROCHLORIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Meclizine Hydrochloride.

Product ID71335-0503_43ac9ba0-83fe-47d0-8a40-3d599540de08
NDC71335-0503
Product TypeHuman Prescription Drug
Proprietary NameMECLIZINE HYDROCHLORIDE
Generic NameMeclizine Hydrocloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-06-04
Marketing CategoryANDA / ANDA
Application NumberANDA040659
Labeler NameBryant Ranch Prepack
Substance NameMECLIZINE HYDROCHLORIDE
Active Ingredient Strength25 mg/1
Pharm ClassesAntiemetic [EPC],Emesis Suppression [PE]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0503-0

14 TABLET in 1 BOTTLE (71335-0503-0)
Marketing Start Date2022-02-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0503-3 [71335050303]

MECLIZINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA040659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-28
Marketing End Date2019-02-28

NDC 71335-0503-7 [71335050307]

MECLIZINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA040659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-28
Marketing End Date2019-02-28

NDC 71335-0503-8 [71335050308]

MECLIZINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA040659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-28
Marketing End Date2019-02-28

NDC 71335-0503-2 [71335050302]

MECLIZINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA040659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-28
Marketing End Date2019-02-28

NDC 71335-0503-1 [71335050301]

MECLIZINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA040659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-28
Marketing End Date2019-02-28

NDC 71335-0503-6 [71335050306]

MECLIZINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA040659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-28
Marketing End Date2019-02-28

NDC 71335-0503-4 [71335050304]

MECLIZINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA040659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-28
Marketing End Date2019-02-28

NDC 71335-0503-5 [71335050305]

MECLIZINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA040659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-28
Marketing End Date2019-02-28

Drug Details

Active Ingredients

IngredientStrength
MECLIZINE HYDROCHLORIDE25 mg/1

OpenFDA Data

SPL SET ID:6dd657ba-46dc-4106-9f6a-dfa0ecf85752
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 995666
  • 995624

    • Pharmacological Class

    • Antiemetic [EPC]
    • Emesis Suppression [PE]

    NDC Crossover Matching brand name "MECLIZINE HYDROCHLORIDE" or generic name "Meclizine Hydrocloride"

    NDCBrand NameGeneric Name
    0378-5485Meclizine HydrochlorideMeclizine
    0378-5486Meclizine HydrochlorideMeclizine
    0440-1736Meclizine Hydrochloridemeclizine hydrochloride
    0536-1299Meclizine HydrochlorideMeclizine Hydrochloride
    0615-1553Meclizine Hydrochloridemeclizine hydrochloride
    0615-1554Meclizine Hydrochloridemeclizine hydrochloride
    0615-8052Meclizine HydrochlorideMeclizine Hydrochloride
    0615-8224Meclizine HydrochlorideMeclizine Hydrochloride
    0615-8303Meclizine HydrochlorideMeclizine
    0904-6516Meclizine HydrochlorideMeclizine
    0904-6517Meclizine HydrochlorideMeclizine Hydrochloride
    10544-081MECLIZINE HYDROCHLORIDEMeclizine Hydrocloride
    10544-108Meclizine Hydrochloridemeclizine hydrochloride
    12634-424Meclizine HydrochlorideMeclizine Hydrochloride
    16571-660Meclizine HydrochlorideMeclizine Hydrochloride
    16571-661Meclizine HydrochlorideMeclizine Hydrochloride
    16571-662Meclizine HydrochlorideMeclizine Hydrochloride
    16571-663Meclizine HydrochlorideMeclizine Hydrochloride
    21695-237Meclizine HydrochlorideMeclizine Hydrochloride
    21695-383Meclizine HydrochlorideMeclizine Hydrochloride
    24689-138Meclizine HydrochlorideMeclizine Hydrochloride
    24689-139Meclizine HydrochlorideMeclizine Hydrochloride
    24689-146Meclizine HydrochlorideMeclizine Hydrochloride
    33261-718MECLIZINE HYDROCHLORIDEMeclizine Hydrocloride
    35356-901MECLIZINE HYDROCHLORIDEMeclizine Hydrochloride
    68071-3017MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    68071-3308MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    68071-4299Meclizine HydrochlorideMeclizine Hydrochloride
    68071-4488MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    68071-4352Meclizine HydrochlorideMeclizine Hydrochloride
    68071-4694MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    68071-4372Meclizine HydrochlorideMeclizine Hydrochloride
    68071-4497Meclizine HydrochlorideMeclizine Hydrochloride
    68084-490Meclizine HydrochlorideMeclizine Hydrochloride
    68084-491Meclizine HydrochlorideMeclizine Hydrochloride
    69677-153Meclizine HydrochlorideMeclizine Hydrochloride
    70518-0447MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    70518-0421Meclizine HydrochlorideMeclizine Hydrochloride
    70518-0422Meclizine HydrochlorideMeclizine Hydrochloride
    70518-1308MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    70518-1402Meclizine HydrochlorideMeclizine Hydrochloride
    70934-138Meclizine HydrochlorideMeclizine Hydrochloride
    71335-0732Meclizine HydrochlorideMeclizine Hydrochloride
    71335-0814Meclizine HydrochlorideMeclizine Hydrochloride
    71335-0153MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    71335-0189Meclizine HydrochlorideMeclizine Hydrochloride
    71335-0503MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    75921-121MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    35356-914MECLIZINE HYDROCHLORIDEMECLIZINE HYDROCHLORIDE
    42291-609Meclizine HydrochlorideMeclizine Hydrochloride
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