trandolapril and verapamil hydrochloride

Generic: trandolapril and verapamil hydrochloride

Labeler: glenmark pharmaceuticals inc., usa
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trandolapril and verapamil hydrochloride
Generic Name trandolapril and verapamil hydrochloride
Labeler glenmark pharmaceuticals inc., usa
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

trandolapril 2 mg/1, verapamil hydrochloride 180 mg/1

Manufacturer
Glenmark Pharmaceuticals Inc., USA

Identifiers & Regulatory

Product NDC 68462-295
Product ID 68462-295_770b4914-a475-4841-83f8-79261f115eff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079135
Listing Expiration 2027-12-31
Marketing Start 2015-02-25

Pharmacologic Class

Established (EPC)
angiotensin converting enzyme inhibitor [epc]
Mechanism of Action
angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68462295
Hyphenated Format 68462-295

Supplemental Identifiers

RxCUI
897781 897783 897844 897853
UPC
0368462294017 0368462329016
UNII
V3888OEY5R 1T0N3G9CRC
NUI
N0000175562 N0000000181

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 trandolapril and verapamil hydrochloride (source: ndc)
Generic Name trandolapril and verapamil hydrochloride (source: ndc)
Application Number ANDA079135 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
  • 180 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-01)
  • 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-10)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-90)
source: ndc

Packages (3)

Ingredients (2)

trandolapril (2 mg/1) verapamil hydrochloride (180 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "770b4914-a475-4841-83f8-79261f115eff", "openfda": {"nui": ["N0000175562", "N0000000181"], "upc": ["0368462294017", "0368462329016"], "unii": ["V3888OEY5R", "1T0N3G9CRC"], "rxcui": ["897781", "897783", "897844", "897853"], "spl_set_id": ["39bad727-af4c-4d20-933b-7f287e88099a"], "pharm_class_epc": ["Angiotensin Converting Enzyme Inhibitor [EPC]"], "pharm_class_moa": ["Angiotensin-converting Enzyme Inhibitors [MoA]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-01)", "package_ndc": "68462-295-01", "marketing_start_date": "20150225"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-10)", "package_ndc": "68462-295-10", "marketing_start_date": "20150225"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-295-90)", "package_ndc": "68462-295-90", "marketing_start_date": "20150225"}], "brand_name": "Trandolapril and Verapamil Hydrochloride", "product_id": "68462-295_770b4914-a475-4841-83f8-79261f115eff", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Cytochrome P450 3A4 Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "product_ndc": "68462-295", "generic_name": "Trandolapril and Verapamil Hydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trandolapril and Verapamil Hydrochloride", "active_ingredients": [{"name": "TRANDOLAPRIL", "strength": "2 mg/1"}, {"name": "VERAPAMIL HYDROCHLORIDE", "strength": "180 mg/1"}], "application_number": "ANDA079135", "marketing_category": "ANDA", "marketing_start_date": "20150225", "listing_expiration_date": "20271231"}