sildenafil citrate
Generic: sildenafil citrate
Labeler: zydus pharmaceuticals (usa) inc.Drug Facts
Product Profile
Brand Name
sildenafil citrate
Generic Name
sildenafil citrate
Labeler
zydus pharmaceuticals (usa) inc.
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
sildenafil citrate 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70710-1716
Product ID
70710-1716_b42790ec-b9ad-4b34-b98d-dfb8d246eff2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215708
Listing Expiration
2027-12-31
Marketing Start
2022-10-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707101716
Hyphenated Format
70710-1716
Supplemental Identifiers
RxCUI
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 citrate (source: ndc)
Generic Name
sildenafil citrate (source: ndc)
Application Number
ANDA215708 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 BOTTLE, GLASS in 1 CARTON (70710-1716-4) / 112 mL in 1 BOTTLE, GLASS
- 1 BOTTLE, PLASTIC in 1 CARTON (70710-1716-5) / 112 mL in 1 BOTTLE, PLASTIC
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b42790ec-b9ad-4b34-b98d-dfb8d246eff2", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["1307427"], "spl_set_id": ["b2f04ce4-f19c-403d-8a83-74f123e5d30a"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (70710-1716-4) / 112 mL in 1 BOTTLE, GLASS", "package_ndc": "70710-1716-4", "marketing_start_date": "20221027"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (70710-1716-5) / 112 mL in 1 BOTTLE, PLASTIC", "package_ndc": "70710-1716-5", "marketing_start_date": "20221027"}], "brand_name": "Sildenafil Citrate", "product_id": "70710-1716_b42790ec-b9ad-4b34-b98d-dfb8d246eff2", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "70710-1716", "generic_name": "Sildenafil Citrate", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "10 mg/mL"}], "application_number": "ANDA215708", "marketing_category": "ANDA", "marketing_start_date": "20221027", "listing_expiration_date": "20271231"}