telmisartan and hydrochlorothiazide
Generic: telmisartan and hydrochlorothiazide
Labeler: alembic pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
telmisartan and hydrochlorothiazide
Generic Name
telmisartan and hydrochlorothiazide
Labeler
alembic pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
hydrochlorothiazide 25 mg/1, telmisartan 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62332-211
Product ID
62332-211_ef7e32c5-7fa8-4179-927e-79d19a6f449e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203010
Listing Expiration
2026-12-31
Marketing Start
2016-06-25
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62332211
Hyphenated Format
62332-211
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
telmisartan and hydrochlorothiazide (source: ndc)
Generic Name
telmisartan and hydrochlorothiazide (source: ndc)
Application Number
ANDA203010 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 80 mg/1
Packaging
- 100 TABLET in 1 CARTON (62332-211-10)
- 30 TABLET in 1 BOTTLE (62332-211-30)
- 1000 TABLET in 1 BOTTLE (62332-211-91)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef7e32c5-7fa8-4179-927e-79d19a6f449e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0362332210305", "0362332211302"], "unii": ["0J48LPH2TH", "U5SYW473RQ"], "rxcui": ["283316", "283317", "477130"], "spl_set_id": ["e80f232c-c1c4-4524-a0a5-d23ee0d1f3b7"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (62332-211-10)", "package_ndc": "62332-211-10", "marketing_start_date": "20160625"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-211-30)", "package_ndc": "62332-211-30", "marketing_start_date": "20160625"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-211-91)", "package_ndc": "62332-211-91", "marketing_start_date": "20160625"}], "brand_name": "Telmisartan and Hydrochlorothiazide", "product_id": "62332-211_ef7e32c5-7fa8-4179-927e-79d19a6f449e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "62332-211", "generic_name": "Telmisartan and Hydrochlorothiazide", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "TELMISARTAN", "strength": "80 mg/1"}], "application_number": "ANDA203010", "marketing_category": "ANDA", "marketing_start_date": "20160625", "listing_expiration_date": "20261231"}