valsartan

Generic: valsartan

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

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valsartan 40 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-151
Product ID 31722-151_4b026ec3-7e85-69ee-e063-6394a90a8c7f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203311
Listing Expiration 2027-12-31
Marketing Start 2021-06-23

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 31722151
Hyphenated Format 31722-151

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UPC
0331722151306 0331722154307 0331722153300 0331722152327
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 ANDA203311 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (31722-151-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (31722-151-30)
  • 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-151-31)
  • 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-151-32)
  • 90 TABLET, FILM COATED in 1 BOTTLE (31722-151-90)
source: ndc

Packages (5)

31722-151-05 500 TABLET, FILM COATED in 1 BOTTLE (31722-151-05) 31722-151-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-151-30) 31722-151-31 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-151-31) 31722-151-32 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-151-32) 31722-151-90 90 TABLET, FILM COATED in 1 BOTTLE (31722-151-90)

Ingredients (1)

valsartan (40 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": "4b026ec3-7e85-69ee-e063-6394a90a8c7f", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0331722151306", "0331722154307", "0331722153300", "0331722152327"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["d6e84105-9394-4ef0-928c-20d07d3fbaa9"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-151-05)", "package_ndc": "31722-151-05", "marketing_start_date": "20210623"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-151-30)", "package_ndc": "31722-151-30", "marketing_start_date": "20210623"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (31722-151-31)", "package_ndc": "31722-151-31", "marketing_start_date": "20210623"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-151-32)", "package_ndc": "31722-151-32", "marketing_start_date": "20210623"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-151-90)", "package_ndc": "31722-151-90", "marketing_start_date": "20210623"}], "brand_name": "Valsartan", "product_id": "31722-151_4b026ec3-7e85-69ee-e063-6394a90a8c7f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "31722-151", "generic_name": "Valsartan", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "40 mg/1"}], "application_number": "ANDA203311", "marketing_category": "ANDA", "marketing_start_date": "20210623", "listing_expiration_date": "20271231"}