valsartan
Generic: valsartan
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
valsartan
Generic Name
valsartan
Labeler
camber pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
valsartan 320 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
31722-748
Product ID
31722-748_2b44fd7a-fd5a-984d-e063-6294a90a3fff
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203311
Listing Expiration
2026-12-31
Marketing Start
2015-01-05
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722748
Hyphenated Format
31722-748
Supplemental Identifiers
RxCUI
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
valsartan (source: ndc)
Generic Name
valsartan (source: ndc)
Application Number
ANDA203311 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 320 mg/1
Packaging
- 500 TABLET, FILM COATED in 1 BOTTLE (31722-748-05)
- 30 TABLET, FILM COATED in 1 BOTTLE (31722-748-30)
- 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-748-31)
- 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-748-32)
- 90 TABLET, FILM COATED in 1 BOTTLE (31722-748-90)
Packages (5)
31722-748-05
500 TABLET, FILM COATED in 1 BOTTLE (31722-748-05)
31722-748-30
30 TABLET, FILM COATED in 1 BOTTLE (31722-748-30)
31722-748-31
10 TABLET, FILM COATED in 1 BLISTER PACK (31722-748-31)
31722-748-32
100 TABLET, FILM COATED in 1 BLISTER PACK (31722-748-32)
31722-748-90
90 TABLET, FILM COATED in 1 BOTTLE (31722-748-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b44fd7a-fd5a-984d-e063-6294a90a3fff", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["0ff36e83-b307-42db-a2ab-bae3f6805c20"], "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 (31722-748-05)", "package_ndc": "31722-748-05", "marketing_start_date": "20150105"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-748-30)", "package_ndc": "31722-748-30", "marketing_start_date": "20150105"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (31722-748-31)", "package_ndc": "31722-748-31", "marketing_start_date": "20150105"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-748-32)", "package_ndc": "31722-748-32", "marketing_start_date": "20150105"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-748-90)", "package_ndc": "31722-748-90", "marketing_start_date": "20150105"}], "brand_name": "Valsartan", "product_id": "31722-748_2b44fd7a-fd5a-984d-e063-6294a90a3fff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "31722-748", "generic_name": "Valsartan", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA203311", "marketing_category": "ANDA", "marketing_start_date": "20150105", "listing_expiration_date": "20261231"}