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, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 50 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1844
Product ID 70518-1844_4977420c-2205-90c0-e063-6294a90a898d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202659
Listing Expiration 2027-12-31
Marketing Start 2019-02-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181844
Hyphenated Format 70518-1844

Supplemental Identifiers

RxCUI
312950
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 ANDA202659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1844-1)
source: ndc

Packages (1)

70518-1844-1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1844-1)

Ingredients (1)

sildenafil citrate (50 mg/1)

Linked Drug Pages (1)

Sildenafil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4977420c-2205-90c0-e063-6294a90a898d", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["99bc66a4-05d1-4372-a25a-1153d7af580e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1844-1)", "package_ndc": "70518-1844-1", "marketing_start_date": "20221212"}], "brand_name": "Sildenafil", "product_id": "70518-1844_4977420c-2205-90c0-e063-6294a90a898d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "70518-1844", "generic_name": "Sildenafil", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20190204", "listing_expiration_date": "20271231"}