Excluded / Inactive
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for Sildenafil citrate 100 mg Oral Tablet (RxCUI 314229). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.
Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.
Manufacturer Quick Index
Found 136 manufactured products
A-S Medication Solutions
NDC Product
Human Prescription DrugSildenafil NDC 50090-5325
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Sildenafil NDC 50090-5802
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugSildenafil NDC 50090-7964
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
ANI Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSildenafil Citrate NDC 70954-407
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 70954-408
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 70954-409
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advagen Pharma Ltd
NDC Product
Human Prescription DrugSildenafil NDC 72888-015
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72888-016
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72888-017
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Advanced Rx of Tennessee, LLC
NDC Product
Human Prescription DrugSildenafil Citrate NDC 80425-0410
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 80425-0503
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Ajanta Pharma USA Inc.
NDC Product
Human Prescription DrugSildenafil Citrate NDC 27241-067
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 27241-068
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 27241-069
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Amneal Pharmaceuticals NY LLC
NDC Product
Human Prescription DrugSildenafil NDC 60219-1751
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 60219-1752
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 60219-1753
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aphena Pharma Solutions - Tennessee, LLC
NDC Product
Viagra NDC 67544-355
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Viagra NDC 67544-356
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Human Prescription DrugSildenafil NDC 71610-675
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 71610-679
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Appco Pharma LLC
NDC Product
Human Prescription DrugSildenafil NDC 55801-338
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 55801-339
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 55801-340
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Asclemed USA, Inc.
NDC Product
Human Prescription DrugSildenafil Citrate NDC 76420-563
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 76420-564
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 76420-565
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Aurobindo Pharma Limited
NDC Product
Human Prescription DrugSildenafil NDC 65862-689
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 65862-690
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 65862-691
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bostal LLC
NDC Product
Human Prescription DrugSildenafil NDC 35561-251
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 35561-252
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 35561-253
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Bryant Ranch Prepack
NDC Product
Human Prescription DrugSildenafil NDC 71335-0969
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Sildenafil NDC 71335-1088
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 71335-1088
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 71335-1437
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 71335-1777
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 71335-3049
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
CIPLA USA INC.,
NDC Product
Human Prescription DrugSildenafil NDC 69097-951
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 69097-952
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 69097-953
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Cadila Pharmaceuticals Limited
NDC Product
Human Prescription DrugSildenafil NDC 71209-106
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 71209-107
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 71209-108
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Camber Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSildenafil NDC 31722-709
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 31722-710
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 31722-711
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 31722-965
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 31722-966
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 31722-967
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
DIRECT RX
NDC Product
Human Prescription DrugSildenafil NDC 72189-069
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Exelan Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSildenafil NDC 76282-643
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 76282-644
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 76282-645
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
H.J. Harkins Company, Inc.
NDC Product
Sildenafil NDC 76519-1216
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Sildenafil NDC 76519-1218
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
HEC Pharm USA Inc.
NDC Product
Human Prescription DrugSildenafil NDC 72303-0845
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72303-0846
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72303-0847
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Macleods Pharmaceuticals Limited
NDC Product
Human Prescription DrugSildenafil NDC 33342-041
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 33342-042
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 33342-043
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Modavar Pharmaceuticals LLC
NDC Product
Human Prescription DrugSildenafil NDC 72241-069
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72241-070
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72241-071
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Mylan Pharmaceuticals Inc.
NDC Product
Human Prescription DrugSildenafil Citrate NDC 59762-0034
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 59762-0035
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 59762-0036
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA AUTHORIZED GENERIC
Active Listing
NIVAGEN PHARMACEUTICALS, INC.
NDC Product
Human Prescription DrugSildenafil Citrate NDC 75834-240
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 75834-241
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 75834-272
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northstar Rx LLC
NDC Product
Human Prescription DrugSildenafil Citrate NDC 72603-883
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 72603-884
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 72603-885
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Northwind Health Company, LLC
NDC Product
Human Prescription DrugSildenafil NDC 51655-468
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 51655-794
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSildenafil NDC 68071-3832
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 68071-3862
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NuCare Pharmaceuticals,Inc.
NDC Product
Human Prescription DrugSildenafil NDC 68071-2985
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 68071-3410
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 68071-3549
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 68071-3908
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 68071-4599
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 68071-4617
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
PD-Rx Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSildenafil Citrate NDC 43063-940
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72789-098
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 72789-406
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
PFIZER LABORATORIES DIV PFIZER INC
NDC Product
Human Prescription DrugViagra NDC 0069-4200
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugViagra NDC 0069-4210
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugViagra NDC 0069-4220
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
Physicians Total Care, Inc.
NDC Product
Viagra NDC 54868-4084
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Viagra NDC 54868-4706
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Viagra NDC 54868-4784
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
Preferred Pharmaceuticals Inc.
NDC Product
Human Prescription DrugSildenafil Citrate NDC 68788-4111
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Sildenafil NDC 68788-7218
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Human Prescription DrugSildenafil Citrate NDC 68788-8301
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 68788-8804
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
Preferred Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugSildenafil NDC 68788-7879
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Proficient Rx LP
NDC Product
Human Prescription DrugSildenafil NDC 71205-088
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 71205-220
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 71205-231
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 71205-473
- Generic Name
- Sildenafil
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 71205-498
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 71205-657
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 82804-025
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Quallent Pharmaceuticals Health LLC
NDC Product
Human Prescription DrugSildenafil Citrate NDC 82009-093
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Reyoung Corporation
NDC Product
Human Prescription DrugSildenafil NDC 82647-210
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 82647-211
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 82647-212
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Teva Pharmaceuticals USA, Inc.
NDC Product
Human Prescription DrugSildenafil NDC 0093-5341
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 0093-5342
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 0093-5343
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Torrent Pharmaceuticals Limited
NDC Product
Human Prescription DrugSildenafil Citrate NDC 13668-186
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 13668-187
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 13668-188
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
TruPharma LLC
NDC Product
Human Prescription DrugSildenafil NDC 52817-340
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 52817-341
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 52817-342
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Umedica Laboratories USA Inc.
NDC Product
Human Prescription DrugSildenafil Citrate NDC 60290-002
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 60290-003
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil Citrate NDC 60290-079
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
Unit Dose Services
NDC Product
Sildenafil Citrate NDC 50436-0035
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Sildenafil Citrate NDC 50436-0036
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- NDA
Excluded / Inactive
NDC Product
Sildenafil NDC 50436-0710
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Sildenafil NDC 50436-0711
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Viatris Specialty LLC
NDC Product
Human Prescription DrugViagra NDC 58151-426
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugViagra NDC 58151-427
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugViagra NDC 58151-428
- Generic Name
- Sildenafil Citrate
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- NDA
Active Listing
XLCARE Pharmaceuticals INC.
NDC Product
Human Prescription DrugSildenafil NDC 72865-101
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72865-102
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugSildenafil NDC 72865-103
- Generic Name
- Sildenafil
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Marketing
- ANDA
Active Listing
medsource pharmaceuticals
NDC Product
Sildenafil Citrate NDC 45865-937
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
