sildenafil

Generic: sildenafil

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sildenafil citrate 20 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3433
Product ID 70518-3433_485bc9db-8666-9f5a-e063-6394a90a7921
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210394
Listing Expiration 2027-12-31
Marketing Start 2022-06-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183433
Hyphenated Format 70518-3433

Supplemental Identifiers

RxCUI
577033
UNII
BW9B0ZE037

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 ANDA210394 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 POUCH in 1 BOX (70518-3433-0) / 1 TABLET in 1 POUCH (70518-3433-1)
  • 360 POUCH in 1 BOX (70518-3433-2) / 1 TABLET in 1 POUCH (70518-3433-1)
  • 180 POUCH in 1 BOX (70518-3433-4) / 1 TABLET in 1 POUCH (70518-3433-1)
source: ndc

Packages (3)

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": "485bc9db-8666-9f5a-e063-6394a90a7921", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["e4f41e9e-d508-4f91-8677-8a19b07139de"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-3433-0)  / 1 TABLET in 1 POUCH (70518-3433-1)", "package_ndc": "70518-3433-0", "marketing_start_date": "20220609"}, {"sample": false, "description": "360 POUCH in 1 BOX (70518-3433-2)  / 1 TABLET in 1 POUCH (70518-3433-1)", "package_ndc": "70518-3433-2", "marketing_start_date": "20220609"}, {"sample": false, "description": "180 POUCH in 1 BOX (70518-3433-4)  / 1 TABLET in 1 POUCH (70518-3433-1)", "package_ndc": "70518-3433-4", "marketing_start_date": "20240110"}], "brand_name": "Sildenafil", "product_id": "70518-3433_485bc9db-8666-9f5a-e063-6394a90a7921", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "70518-3433", "generic_name": "Sildenafil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA210394", "marketing_category": "ANDA", "marketing_start_date": "20220609", "listing_expiration_date": "20271231"}