sildenafil
Generic: sildenafil
Labeler: ajanta pharma usa inc.Drug Facts
Product Profile
Brand Name
sildenafil
Generic Name
sildenafil
Labeler
ajanta pharma usa inc.
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
sildenafil citrate 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
27241-175
Product ID
27241-175_f6bcdef0-843c-4478-aa14-42beaf99c538
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212883
Listing Expiration
2026-12-31
Marketing Start
2019-11-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
27241175
Hyphenated Format
27241-175
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
ANDA212883 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 POUCH in 1 CARTON (27241-175-29) / 1 BOTTLE in 1 POUCH / 112 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f6bcdef0-843c-4478-aa14-42beaf99c538", "openfda": {"upc": ["0327241175299"], "unii": ["BW9B0ZE037"], "rxcui": ["1307427"], "spl_set_id": ["283790ed-2acb-4714-a0af-b348bb642785"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (27241-175-29) / 1 BOTTLE in 1 POUCH / 112 mL in 1 BOTTLE", "package_ndc": "27241-175-29", "marketing_start_date": "20191127"}], "brand_name": "Sildenafil", "product_id": "27241-175_f6bcdef0-843c-4478-aa14-42beaf99c538", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "27241-175", "generic_name": "Sildenafil", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "10 mg/mL"}], "application_number": "ANDA212883", "marketing_category": "ANDA", "marketing_start_date": "20191127", "listing_expiration_date": "20261231"}