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NDC 71205-0231-20 Sildenafil Citrate 100 mg/1 Details
Sildenafil Citrate 100 mg/1
Sildenafil Citrate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is SILDENAFIL CITRATE.
Product Information
NDC | 71205-0231 |
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Product ID | 71205-231_bd0158fe-7fca-44c0-9a6c-36fb5c489114 |
Associated GPIs | 40304070100330 |
GCN Sequence Number | 039191 |
GCN Sequence Number Description | sildenafil citrate TABLET 100 MG ORAL |
HIC3 | F2A |
HIC3 Description | DRUGS TO TREAT ERECTILE DYSFUNCTION (ED) |
GCN | 57903 |
HICL Sequence Number | 018084 |
HICL Sequence Number Description | SILDENAFIL CITRATE |
Brand/Generic | Generic |
Proprietary Name | Sildenafil Citrate |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Sildenafil |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 100 |
Active Ingredient Units | mg/1 |
Substance Name | SILDENAFIL CITRATE |
Labeler Name | Proficient Rx LP |
Pharmaceutical Class | Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA091448 |
Listing Certified Through | 2024-12-31 |
Package
NDC 71205-0231-20 (71205023120)
NDC Package Code | 71205-231-20 |
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Billing NDC | 71205023120 |
Package | 20 TABLET, FILM COATED in 1 BOTTLE (71205-231-20) |
Marketing Start Date | 2023-10-19 |
NDC Exclude Flag | N |
Pricing Information | N/A |