Package 16571-661-01
Brand: meclizine hydrochloride
Generic: meclizine hydrochloridePackage Facts
Identity
Package NDC
16571-661-01
Digits Only
1657166101
Product NDC
16571-661
Description
100 TABLET in 1 BOTTLE (16571-661-01)
Marketing
Marketing Status
Brand
meclizine hydrochloride
Generic
meclizine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be27ea6-3d0a-4036-ab42-fea4720daa34", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995632", "995666", "995686"], "spl_set_id": ["c9ddc39c-bc6b-42f1-8c5f-5aff2d79c4bd"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-661-01)", "package_ndc": "16571-661-01", "marketing_start_date": "20200115"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16571-661-10)", "package_ndc": "16571-661-10", "marketing_start_date": "20200115"}], "brand_name": "Meclizine Hydrochloride", "product_id": "16571-661_2be27ea6-3d0a-4036-ab42-fea4720daa34", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "16571-661", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "NDA010721", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}