sildenafil
Generic: sildenafil
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
sildenafil
Generic Name
sildenafil
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sildenafil citrate 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1638
Product ID
71335-1638_68ec1574-866c-495a-a4e9-5631d24b2b04
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203814
Listing Expiration
2026-12-31
Marketing Start
2014-01-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351638
Hyphenated Format
71335-1638
Supplemental Identifiers
RxCUI
UNII
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
ANDA203814 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-1638-1)
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1638-2)
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-1638-3)
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1638-4)
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1638-5)
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1638-6)
- 270 TABLET, FILM COATED in 1 BOTTLE (71335-1638-7)
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-1638-8)
- 12 TABLET, FILM COATED in 1 BOTTLE (71335-1638-9)
Packages (9)
71335-1638-1
10 TABLET, FILM COATED in 1 BOTTLE (71335-1638-1)
71335-1638-2
30 TABLET, FILM COATED in 1 BOTTLE (71335-1638-2)
71335-1638-3
7 TABLET, FILM COATED in 1 BOTTLE (71335-1638-3)
71335-1638-4
90 TABLET, FILM COATED in 1 BOTTLE (71335-1638-4)
71335-1638-5
60 TABLET, FILM COATED in 1 BOTTLE (71335-1638-5)
71335-1638-6
20 TABLET, FILM COATED in 1 BOTTLE (71335-1638-6)
71335-1638-7
270 TABLET, FILM COATED in 1 BOTTLE (71335-1638-7)
71335-1638-8
15 TABLET, FILM COATED in 1 BOTTLE (71335-1638-8)
71335-1638-9
12 TABLET, FILM COATED in 1 BOTTLE (71335-1638-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "68ec1574-866c-495a-a4e9-5631d24b2b04", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["85767ed7-932b-4e2b-8bba-b59bb45ce116"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-1638-1)", "package_ndc": "71335-1638-1", "marketing_start_date": "20140103"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1638-2)", "package_ndc": "71335-1638-2", "marketing_start_date": "20140103"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71335-1638-3)", "package_ndc": "71335-1638-3", "marketing_start_date": "20140103"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1638-4)", "package_ndc": "71335-1638-4", "marketing_start_date": "20140103"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1638-5)", "package_ndc": "71335-1638-5", "marketing_start_date": "20140103"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-1638-6)", "package_ndc": "71335-1638-6", "marketing_start_date": "20140103"}, {"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE (71335-1638-7)", "package_ndc": "71335-1638-7", "marketing_start_date": "20140103"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-1638-8)", "package_ndc": "71335-1638-8", "marketing_start_date": "20140103"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (71335-1638-9)", "package_ndc": "71335-1638-9", "marketing_start_date": "20140103"}], "brand_name": "Sildenafil", "product_id": "71335-1638_68ec1574-866c-495a-a4e9-5631d24b2b04", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-1638", "generic_name": "Sildenafil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203814", "marketing_category": "ANDA", "marketing_start_date": "20140103", "listing_expiration_date": "20261231"}