meclizine hydrochloride
Generic: meclizine hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
meclizine hydrochloride
Generic Name
meclizine hydrochloride
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
meclizine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-730
Product ID
60687-730_38437b2a-bc23-c6d7-e063-6294a90ac5db
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201451
Listing Expiration
2026-12-31
Marketing Start
2023-04-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687730
Hyphenated Format
60687-730
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
meclizine hydrochloride (source: ndc)
Generic Name
meclizine hydrochloride (source: ndc)
Application Number
ANDA201451 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (60687-730-01) / 1 TABLET in 1 BLISTER PACK (60687-730-11)
- 50 BLISTER PACK in 1 CARTON (60687-730-65) / 1 TABLET in 1 BLISTER PACK (60687-730-11)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38437b2a-bc23-c6d7-e063-6294a90ac5db", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995666"], "spl_set_id": ["af1e45ca-1478-4eeb-8fdc-4f3d3eda4ed5"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-730-01) / 1 TABLET in 1 BLISTER PACK (60687-730-11)", "package_ndc": "60687-730-01", "marketing_start_date": "20230420"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (60687-730-65) / 1 TABLET in 1 BLISTER PACK (60687-730-11)", "package_ndc": "60687-730-65", "marketing_start_date": "20240207"}], "brand_name": "Meclizine Hydrochloride", "product_id": "60687-730_38437b2a-bc23-c6d7-e063-6294a90ac5db", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "60687-730", "generic_name": "Meclizine Hydrochloride", "labeler_name": "American Health Packaging", "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": "20230420", "listing_expiration_date": "20261231"}