Package 51655-175-52

Brand: meclizine hydrochloride

Generic: meclizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-175-52
Digits Only 5165517552
Product NDC 51655-175
Product ID 51655-175_48c40e56-3176-62df-e063-6294a90a23c8
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-175-52)

Marketing

Marketing Status
Marketed Since 2022-10-07
Brand meclizine hydrochloride
Generic meclizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Meclizine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48c40e56-3176-62df-e063-6294a90a23c8", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["f2b4716c-411a-62cd-e053-2a95a90a6f4b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-175-52)", "package_ndc": "51655-175-52", "marketing_start_date": "20221007"}], "brand_name": "Meclizine Hydrochloride", "product_id": "51655-175_48c40e56-3176-62df-e063-6294a90a23c8", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "51655-175", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA201451", "marketing_category": "ANDA", "marketing_start_date": "20221007", "listing_expiration_date": "20271231"}