Package 71335-0879-1

Brand: cartia xt

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0879-1
Digits Only 7133508791
Product NDC 71335-0879
Product ID 71335-0879_053455c6-3889-4a52-9981-db90a6bce8ed
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-1)

Marketing

Marketing Status
Marketed Since 2018-06-25
Brand cartia xt
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

Cartia XT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "053455c6-3889-4a52-9981-db90a6bce8ed", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830845", "831255"], "spl_set_id": ["e02f5fad-6482-4d5d-91c5-0ae6b0ce15b8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-1)", "package_ndc": "71335-0879-1", "marketing_start_date": "20180625"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-2)", "package_ndc": "71335-0879-2", "marketing_start_date": "20211227"}], "brand_name": "Cartia XT", "product_id": "71335-0879_053455c6-3889-4a52-9981-db90a6bce8ed", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "71335-0879", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cartia", "brand_name_suffix": "XT", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA074752", "marketing_category": "ANDA", "marketing_start_date": "19980709", "listing_expiration_date": "20261231"}