diltiazem hydrochloride

Generic: diltiazem hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride
Generic Name diltiazem hydrochloride
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 60 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-728
Product ID 60687-728_437e5fb1-aebc-9dd7-e063-6294a90ad921
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074185
Listing Expiration 2026-12-31
Marketing Start 2023-12-01

Pharmacologic Class

Classes
calcium channel antagonists [moa] calcium channel blocker [epc] cytochrome p450 3a4 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687728
Hyphenated Format 60687-728

Supplemental Identifiers

RxCUI
831103 833217
UNII
OLH94387TE

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name diltiazem hydrochloride (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number ANDA074185 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-728-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-728-11)
source: ndc

Packages (1)

60687-728-01 100 BLISTER PACK in 1 CARTON (60687-728-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-728-11)

Ingredients (1)

diltiazem hydrochloride (60 mg/1)

Linked Drug Pages (1)

Diltiazem Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "437e5fb1-aebc-9dd7-e063-6294a90ad921", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["831103", "833217"], "spl_set_id": ["14869f9e-6a66-4f75-b0fc-4d808b1ee85e"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-728-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-728-11)", "package_ndc": "60687-728-01", "marketing_start_date": "20231201"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "60687-728_437e5fb1-aebc-9dd7-e063-6294a90ad921", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "60687-728", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA074185", "marketing_category": "ANDA", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}