Product NDC: | 49884-071 |
Proprietary Name: | RIBASPHERE RibaPak |
Non Proprietary Name: | ribavirin |
Active Ingredient(s): | & nbsp; ribavirin |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49884-071 |
Labeler Name: | PAR Pharmaceutical Companies, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077456 |
Marketing Category: | ANDA |
Start Marketing Date: | 20051206 |
Package NDC: | 49884-071-76 |
Package Description: | 4 DOSE PACK in 1 CARTON (49884-071-76) > 1 KIT in 1 DOSE PACK (49884-071-41) |
NDC Code | 49884-071-76 |
Proprietary Name | RIBASPHERE RibaPak |
Package Description | 4 DOSE PACK in 1 CARTON (49884-071-76) > 1 KIT in 1 DOSE PACK (49884-071-41) |
Product NDC | 49884-071 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ribavirin |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20051206 |
Marketing Category Name | ANDA |
Labeler Name | PAR Pharmaceutical Companies, Inc. |
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