sildenafil citrate
Generic: sildenafil citrate
Labeler: ani pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
sildenafil citrate
Generic Name
sildenafil citrate
Labeler
ani pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
sildenafil citrate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70954-408
Product ID
70954-408_6d8dbaa6-d61a-46ae-a641-f664104f4714
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216383
Listing Expiration
2026-12-31
Marketing Start
2023-08-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70954408
Hyphenated Format
70954-408
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 citrate (source: ndc)
Generic Name
sildenafil citrate (source: ndc)
Application Number
ANDA216383 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (70954-408-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6d8dbaa6-d61a-46ae-a641-f664104f4714", "openfda": {"upc": ["0370954409106", "0370954407102", "0370954408109"], "unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["6d8dbaa6-d61a-46ae-a641-f664104f4714"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70954-408-10)", "package_ndc": "70954-408-10", "marketing_start_date": "20230829"}], "brand_name": "Sildenafil Citrate", "product_id": "70954-408_6d8dbaa6-d61a-46ae-a641-f664104f4714", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "70954-408", "generic_name": "Sildenafil Citrate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA216383", "marketing_category": "ANDA", "marketing_start_date": "20230829", "listing_expiration_date": "20261231"}