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"68084-622-21" National Drug Code (NDC)
Sildenafil Citrate 3 BLISTER PACK in 1 CARTON (68084-622-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-622-11)
(American Health Packaging)
NDC Code
68084-622-21
Package Description
3 BLISTER PACK in 1 CARTON (68084-622-21) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-622-11)
Product NDC
68084-622
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sildenafil Citrate
Non-Proprietary Name
Sildenafil Citrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20121214
Marketing Category Name
ANDA
Application Number
ANDA091379
Manufacturer
American Health Packaging
Substance Name
SILDENAFIL CITRATE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68084-622-21