Package 47335-671-13

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 47335-671-13
Digits Only 4733567113
Product NDC 47335-671
Description

500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-671-13)

Marketing

Marketing Status
Marketed Since 2010-11-15
Brand diltiazem hydrochloride
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ecddf1f1-b8e7-4a08-8f00-6cc484092a5f", "openfda": {"upc": ["0347335672831", "0347335673838", "0347335671834"], "unii": ["OLH94387TE"], "rxcui": ["830795", "830801", "830837", "830845", "830861"], "spl_set_id": ["eebf29fe-ce22-4482-b850-5854550bf2c4"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-671-13)", "package_ndc": "47335-671-13", "marketing_start_date": "20101115"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-671-18)", "package_ndc": "47335-671-18", "marketing_start_date": "20101115"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-671-19)", "package_ndc": "47335-671-19", "marketing_start_date": "20101115"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-671-81)", "package_ndc": "47335-671-81", "marketing_start_date": "20101115"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-671-83)", "package_ndc": "47335-671-83", "marketing_start_date": "20101115"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "47335-671_ecddf1f1-b8e7-4a08-8f00-6cc484092a5f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "47335-671", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "240 mg/1"}], "application_number": "ANDA090421", "marketing_category": "ANDA", "marketing_start_date": "20101115", "listing_expiration_date": "20261231"}