diltiazem hydrochloride
Generic: diltiazem hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
diltiazem hydrochloride
Generic Name
diltiazem hydrochloride
Labeler
a-s medication solutions
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
diltiazem hcl 240 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7815
Product ID
50090-7815_00b16eac-2719-4dfb-b1bc-3f92e0ac930c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075116
Listing Expiration
2026-12-31
Marketing Start
1999-12-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907815
Hyphenated Format
50090-7815
Supplemental Identifiers
RxCUI
UNII
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
ANDA075116 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 240 mg/1
Packaging
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7815-0)
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7815-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "00b16eac-2719-4dfb-b1bc-3f92e0ac930c", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830837"], "spl_set_id": ["090aa3a9-910e-4f96-b748-783109aa96e6"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7815-0)", "package_ndc": "50090-7815-0", "marketing_start_date": "20251209"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7815-1)", "package_ndc": "50090-7815-1", "marketing_start_date": "20251209"}], "brand_name": "Diltiazem Hydrochloride", "product_id": "50090-7815_00b16eac-2719-4dfb-b1bc-3f92e0ac930c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "50090-7815", "generic_name": "Diltiazem Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem Hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HCL", "strength": "240 mg/1"}], "application_number": "ANDA075116", "marketing_category": "ANDA", "marketing_start_date": "19991228", "listing_expiration_date": "20261231"}