sildenafil

Generic: sildenafil

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

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

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
phosphodiesterase 5 inhibitor [epc] phosphodiesterase 5 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722776
Hyphenated Format 31722-776

Supplemental Identifiers

RxCUI
577033
UPC
0331722776905
UNII
BW9B0ZE037

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 sildenafil (source: ndc)
Generic Name sildenafil (source: ndc)
Application Number ANDA203623 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
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)
source: ndc

Packages (6)

Ingredients (1)

sildenafil citrate (20 mg/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"}