valsartan

Generic: valsartan

Labeler: alembic pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler alembic pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

valsartan 320 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-047
Product ID 46708-047_3c6999e0-a1f1-40f0-8a6e-f3513410fd5d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091367
Listing Expiration 2026-12-31
Marketing Start 2015-01-06

Pharmacologic Class

Established (EPC)
angiotensin 2 receptor blocker [epc]
Mechanism of Action
angiotensin 2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46708047
Hyphenated Format 46708-047

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UPC
0346708045302 0346708047306 0346708046309 0346708044305
UNII
80M03YXJ7I
NUI
N0000000070 N0000175561

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 valsartan (source: ndc)
Generic Name valsartan (source: ndc)
Application Number ANDA091367 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 320 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (46708-047-30)
  • 500 TABLET in 1 BOTTLE (46708-047-71)
  • 90 TABLET in 1 BOTTLE (46708-047-90)
  • 1000 TABLET in 1 BOTTLE (46708-047-91)
source: ndc

Packages (4)

46708-047-30 30 TABLET in 1 BOTTLE (46708-047-30) 46708-047-71 500 TABLET in 1 BOTTLE (46708-047-71) 46708-047-90 90 TABLET in 1 BOTTLE (46708-047-90) 46708-047-91 1000 TABLET in 1 BOTTLE (46708-047-91)

Ingredients (1)

valsartan (320 mg/1)

Linked Drug Pages (1)

Valsartan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c6999e0-a1f1-40f0-8a6e-f3513410fd5d", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0346708045302", "0346708047306", "0346708046309", "0346708044305"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["6e2cd953-88bf-4094-8ba8-2c9ba020f4d7"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (46708-047-30)", "package_ndc": "46708-047-30", "marketing_start_date": "20150106"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (46708-047-71)", "package_ndc": "46708-047-71", "marketing_start_date": "20150106"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (46708-047-90)", "package_ndc": "46708-047-90", "marketing_start_date": "20150106"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-047-91)", "package_ndc": "46708-047-91", "marketing_start_date": "20150106"}], "brand_name": "Valsartan", "product_id": "46708-047_3c6999e0-a1f1-40f0-8a6e-f3513410fd5d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "46708-047", "generic_name": "Valsartan", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA091367", "marketing_category": "ANDA", "marketing_start_date": "20150106", "listing_expiration_date": "20261231"}