sildenafil
Generic: sildenafil
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
sildenafil
Generic Name
sildenafil
Labeler
camber pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sildenafil citrate 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
31722-776
Product ID
31722-776_15e66fb9-9c64-563b-e063-6394a90a5194
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203623
Listing Expiration
2026-12-31
Marketing Start
2014-11-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722776
Hyphenated Format
31722-776
Supplemental Identifiers
RxCUI
UPC
UNII
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
sildenafil (source: ndc)
Generic Name
sildenafil (source: ndc)
Application Number
ANDA203623 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 500 TABLET, FILM COATED in 1 BOTTLE (31722-776-05)
- 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-31)
- 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-32)
- 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-33)
- 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-34)
- 90 TABLET, FILM COATED in 1 BOTTLE (31722-776-90)
Packages (6)
31722-776-05
500 TABLET, FILM COATED in 1 BOTTLE (31722-776-05)
31722-776-31
10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-31)
31722-776-32
100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-32)
31722-776-33
10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-33)
31722-776-34
100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-34)
31722-776-90
90 TABLET, FILM COATED in 1 BOTTLE (31722-776-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15e66fb9-9c64-563b-e063-6394a90a5194", "openfda": {"upc": ["0331722776905"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["f9415142-a5ac-45c0-a7c2-fb1fb6751f3d"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-776-05)", "package_ndc": "31722-776-05", "marketing_start_date": "20141126"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-31)", "package_ndc": "31722-776-31", "marketing_start_date": "20141126"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-32)", "package_ndc": "31722-776-32", "marketing_start_date": "20141126"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-33)", "package_ndc": "31722-776-33", "marketing_start_date": "20141126"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-34)", "package_ndc": "31722-776-34", "marketing_start_date": "20141126"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-776-90)", "package_ndc": "31722-776-90", "marketing_start_date": "20141126"}], "brand_name": "Sildenafil", "product_id": "31722-776_15e66fb9-9c64-563b-e063-6394a90a5194", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "31722-776", "generic_name": "Sildenafil", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203623", "marketing_category": "ANDA", "marketing_start_date": "20141126", "listing_expiration_date": "20261231"}