sildenafil

Generic: sildenafil

Labeler: cadila pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler cadila pharmaceuticals limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 100 mg/1

Manufacturer
Cadila Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 71209-108
Product ID 71209-108_eff134c4-3240-4132-b9ea-118ce1fa719a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218045
Listing Expiration 2026-12-31
Marketing Start 2023-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71209108
Hyphenated Format 71209-108

Supplemental Identifiers

RxCUI
312950 314228 314229
UPC
0371209108010 0377209102119 0371209106054 0371209107051 0371209106016 0371209107112 0371209106115
UNII
BW9B0ZE037

Packaging Origin

Original Packager
true

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 ANDA218045 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71209-108-01)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71209-108-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (71209-108-11)
source: ndc

Packages (3)

71209-108-01 30 TABLET, FILM COATED in 1 BOTTLE (71209-108-01) 71209-108-05 100 TABLET, FILM COATED in 1 BOTTLE (71209-108-05) 71209-108-11 1000 TABLET, FILM COATED in 1 BOTTLE (71209-108-11)

Ingredients (1)

sildenafil citrate (100 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": "eff134c4-3240-4132-b9ea-118ce1fa719a", "openfda": {"upc": ["0371209108010", "0377209102119", "0371209106054", "0371209107051", "0371209106016", "0371209107112", "0371209106115"], "unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["c079fc41-7b9a-499d-88ea-86ccb65c828d"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71209-108-01)", "package_ndc": "71209-108-01", "marketing_start_date": "20231201"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71209-108-05)", "package_ndc": "71209-108-05", "marketing_start_date": "20231201"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71209-108-11)", "package_ndc": "71209-108-11", "marketing_start_date": "20231201"}], "brand_name": "Sildenafil", "product_id": "71209-108_eff134c4-3240-4132-b9ea-118ce1fa719a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71209-108", "generic_name": "Sildenafil", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA218045", "marketing_category": "ANDA", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}