tiadylt er

Generic: diltiazem hydrochloride

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tiadylt er
Generic Name diltiazem hydrochloride
Labeler zydus lifesciences limited
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

diltiazem hydrochloride 120 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1035
Product ID 70771-1035_302fc306-6fbe-4567-b5ce-dcc5a45ba894
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206641
Listing Expiration 2026-12-31
Marketing Start 2017-11-08

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 707711035
Hyphenated Format 70771-1035

Supplemental Identifiers

RxCUI
830795 830801 830837 830845 830861 831359 1988308 1988311 1988316 1988319 1988324 1988330
UPC
0370771103997
UNII
OLH94387TE

Packaging Origin

Original Packager
true

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 tiadylt er (source: ndc)
Generic Name diltiazem hydrochloride (source: ndc)
Application Number ANDA206641 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-0)
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-1)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-3)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-5)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-9)
source: ndc

Packages (5)

Ingredients (1)

diltiazem hydrochloride (120 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "302fc306-6fbe-4567-b5ce-dcc5a45ba894", "openfda": {"upc": ["0370771103997"], "unii": ["OLH94387TE"], "rxcui": ["830795", "830801", "830837", "830845", "830861", "831359", "1988308", "1988311", "1988316", "1988319", "1988324", "1988330"], "spl_set_id": ["d88e3546-3984-4dc9-893a-a29e95804550"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-0)", "package_ndc": "70771-1035-0", "marketing_start_date": "20171108"}, {"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-1)", "package_ndc": "70771-1035-1", "marketing_start_date": "20171108"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-3)", "package_ndc": "70771-1035-3", "marketing_start_date": "20171108"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-5)", "package_ndc": "70771-1035-5", "marketing_start_date": "20171108"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1035-9)", "package_ndc": "70771-1035-9", "marketing_start_date": "20171108"}], "brand_name": "TIADYLT ER", "product_id": "70771-1035_302fc306-6fbe-4567-b5ce-dcc5a45ba894", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A4 Inhibitors [MoA]"], "product_ndc": "70771-1035", "generic_name": "diltiazem hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TIADYLT ER", "active_ingredients": [{"name": "DILTIAZEM HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA206641", "marketing_category": "ANDA", "marketing_start_date": "20171108", "listing_expiration_date": "20261231"}