Package 31722-136-31
Brand: sildenafil
Generic: sildenafil powder,Package Facts
Identity
Package NDC
31722-136-31
Digits Only
3172213631
Product NDC
31722-136
Description
1 BOTTLE, GLASS in 1 CARTON (31722-136-31) / 112 mL in 1 BOTTLE, GLASS
Marketing
Marketing Status
Brand
sildenafil
Generic
sildenafil powder,
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1389f9d0-c617-8381-e063-6394a90a7a76", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["1307427"], "spl_set_id": ["598f2b9c-cfb9-4f26-8508-83ca5055c305"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (31722-136-31) / 112 mL in 1 BOTTLE, GLASS", "package_ndc": "31722-136-31", "marketing_start_date": "20210511"}], "brand_name": "Sildenafil", "product_id": "31722-136_1389f9d0-c617-8381-e063-6394a90a7a76", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "31722-136", "generic_name": "Sildenafil Powder,", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "10 mg/mL"}], "application_number": "ANDA213014", "marketing_category": "ANDA", "marketing_start_date": "20210511", "listing_expiration_date": "20261231"}