Package 47335-679-81

Brand: diltiazem hydrochloride

Generic: diltiazem hydrochloride
NDC Package

Package Facts

Identity

Package NDC 47335-679-81
Digits Only 4733567981
Product NDC 47335-679
Product ID 47335-679_3c94f868-93d3-4b36-8420-b2903a0bd79a
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-81)

Marketing

Marketing Status
Marketed Since 2011-10-31
Brand diltiazem hydrochloride
Generic diltiazem hydrochloride
Sample Package No

Linked Drug Pages (1)

Diltiazem Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c94f868-93d3-4b36-8420-b2903a0bd79a", "openfda": {"upc": ["0347335679830", "0347335677836", "0347335676839", "0347335678833", "0347335675832"], "unii": ["OLH94387TE"], "rxcui": ["830795", "830801", "830837", "830845", "830861"], "spl_set_id": ["6f71ba5e-7bd6-409a-80c6-2f22d975aefc"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-13)", "package_ndc": "47335-679-13", "marketing_start_date": "20111031"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-18)", "package_ndc": "47335-679-18", "marketing_start_date": "20111031"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-19)", "package_ndc": "47335-679-19", "marketing_start_date": "20111031"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-81)", "package_ndc": "47335-679-81", "marketing_start_date": "20111031"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-83)", "package_ndc": "47335-679-83", "marketing_start_date": "20111031"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "47335-679_3c94f868-93d3-4b36-8420-b2903a0bd79a", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]"], "product_ndc": "47335-679", "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": "360 mg/1"}], "application_number": "ANDA090492", "marketing_category": "ANDA", "marketing_start_date": "20111031", "listing_expiration_date": "20261231"}