Product ID | 58602-867_21c1f5c5-19fa-4a59-bad3-ea85fd37471b |
NDC | 58602-867 |
Product Type | Human Otc Drug |
Proprietary Name | Ibuprofen and Diphenhydramine Citrate |
Generic Name | Ibuprofen And Diphenhydramine Citrate |
Dosage Form | Tablet, Coated |
Route of Administration | ORAL |
Marketing Start Date | 2022-05-31 |
Marketing Category | ANDA / |
Application Number | ANDA216204 |
Labeler Name | Aurohealth LLC |
Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
Active Ingredient Strength | 38 mg/1; mg/1 |
Pharm Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |