diltiazem hydrochloride extended-release

Generic: diltiazem hydrochloride

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

Drug Facts

Product Profile

Brand Name diltiazem hydrochloride extended-release
Generic Name diltiazem hydrochloride
Labeler american health packaging
Dosage Form CAPSULE, COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 180 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-206
Product ID 60687-206_18597a1d-035b-fba0-e063-6294a90abecf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074984
Listing Expiration 2026-12-31
Marketing Start 2017-01-12

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 60687206
Hyphenated Format 60687-206

Supplemental Identifiers

RxCUI
830801 830837 830845 830861
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 extended-release (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number ANDA074984 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 180 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-206-01) / 1 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-206-11)
source: ndc

Packages (1)

60687-206-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-206-01) / 1 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-206-11)

Ingredients (1)

diltiazem hydrochloride (180 mg/1)

Linked Drug Pages (1)

Diltiazem Hydrochloride Extended-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "18597a1d-035b-fba0-e063-6294a90abecf", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830801", "830837", "830845", "830861"], "spl_set_id": ["11b43a17-8038-462b-8902-259431ad5256"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-206-01)  / 1 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-206-11)", "package_ndc": "60687-206-01", "marketing_start_date": "20170112"}], "brand_name": "Diltiazem Hydrochloride Extended-Release", "product_id": "60687-206_18597a1d-035b-fba0-e063-6294a90abecf", "dosage_form": "CAPSULE, COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "60687-206", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA074984", "marketing_category": "ANDA", "marketing_start_date": "20170112", "listing_expiration_date": "20261231"}