NDC Code | 70000-0602-1 |
Package Description | 40 TABLET in 1 BLISTER PACK (70000-0602-1) |
Product NDC | 70000-0602 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Ibuprofen And Pseudoephedrine Hydrochloride |
Non-Proprietary Name | Ibuprofen And Pseudoephedrine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20220523 |
Marketing Category Name | ANDA |
Application Number | ANDA074567 |
Manufacturer | CARDINAL HEALTH 110, LLC DBA LEADER |
Substance Name | IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength | 200; 30 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC] |