Package 48433-031-20
Brand: diltiazem hydrochloride
Generic: diltiazem hydrochloridePackage Facts
Identity
Package NDC
48433-031-20
Digits Only
4843303120
Product NDC
48433-031
Description
100 BLISTER PACK in 1 CARTON (48433-031-20) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (48433-031-01)
Marketing
Marketing Status
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": "49eef6c8-e1fc-86af-e063-6294a90a0309", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830865", "830869", "830872"], "spl_set_id": ["fc02db0f-5311-4b61-896e-bfe340832735"], "manufacturer_name": ["Safecor Health LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (48433-031-20) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (48433-031-01)", "package_ndc": "48433-031-20", "marketing_start_date": "20260202"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "48433-031_49eef6c8-e1fc-86af-e063-6294a90a0309", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "48433-031", "generic_name": "diltiazem hydrochloride", "labeler_name": "Safecor Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "90 mg/1"}], "application_number": "ANDA074910", "marketing_category": "ANDA", "marketing_start_date": "20260202", "listing_expiration_date": "20271231"}