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 hydrochloride 120 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6328
Product ID
50090-6328_d786e289-37d8-4cb3-9bf0-967fbd5ebc2b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203023
Listing Expiration
2026-12-31
Marketing Start
2018-10-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906328
Hyphenated Format
50090-6328
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
ANDA203023 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 120 mg/1
Packaging
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6328-0)
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6328-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d786e289-37d8-4cb3-9bf0-967fbd5ebc2b", "openfda": {"unii": ["OLH94387TE"], "rxcui": ["830861"], "spl_set_id": ["5460158f-7782-45f4-89b1-f84e6ba178d8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6328-0)", "package_ndc": "50090-6328-0", "marketing_start_date": "20230113"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6328-1)", "package_ndc": "50090-6328-1", "marketing_start_date": "20230113"}], "brand_name": "Diltiazem hydrochloride", "product_id": "50090-6328_d786e289-37d8-4cb3-9bf0-967fbd5ebc2b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]"], "product_ndc": "50090-6328", "generic_name": "Diltiazem hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diltiazem hydrochloride", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA203023", "marketing_category": "ANDA", "marketing_start_date": "20181031", "listing_expiration_date": "20261231"}