Package 67751-166-01

Brand: benadryl ultratabs

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67751-166-01
Digits Only 6775116601
Product NDC 67751-166
Product ID 67751-166_2385ad34-3763-390b-e063-6394a90a12fd
Description

1 POUCH in 1 CARTON (67751-166-01) / 2 TABLET, FILM COATED in 1 POUCH

Marketing

Marketing Status
Marketed Since 2016-09-22
Brand benadryl ultratabs
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Benadryl Ultratabs ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2385ad34-3763-390b-e063-6394a90a12fd", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1049632"], "spl_set_id": ["76433e3c-142c-4704-8b2b-d602f008c377"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (67751-166-01)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67751-166-01", "marketing_start_date": "20160922"}, {"sample": false, "description": "1 POUCH in 1 CARTON (67751-166-02)  / 4 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67751-166-02", "marketing_start_date": "20160922"}], "brand_name": "Benadryl Ultratabs", "product_id": "67751-166_2385ad34-3763-390b-e063-6394a90a12fd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67751-166", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "Navajo Manufacturing Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Ultratabs", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160922", "listing_expiration_date": "20261231"}