Package 49483-329-00

Brand: diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 49483-329-00
Digits Only 4948332900
Product NDC 49483-329
Description

100000 TABLET, COATED in 1 CARTON (49483-329-00)

Marketing

Marketing Status
Marketed Since 2018-12-17
Brand diphenhydramine hydrochloride
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7d3b9a35-9e04-4289-e053-2a91aa0a5042", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["ed899055-0cbb-45bd-92c8-cbef2fc7c361"], "manufacturer_name": ["Time-Cap Labs, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100000 TABLET, COATED in 1 CARTON (49483-329-00)", "package_ndc": "49483-329-00", "marketing_start_date": "20181217"}], "brand_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "product_id": "49483-329_7d3b9a35-9e04-4289-e053-2a91aa0a5042", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "49483-329", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "Time-Cap Labs, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DIPHENHYDRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20100301", "listing_expiration_date": "20261231"}