NDC 69367-199
Doxylamine Succinate and Phenylephrine Hydrochloride
Doxylamine Succinate And Phenylephrine Hydrochloride
Doxylamine Succinate and Phenylephrine Hydrochloride is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Westminster Pharmaceuticals, Llc. The primary component is Doxylamine Succinate; Phenylephrine Hydrochloride.
Product ID | 69367-199_70235edf-e471-4029-9af1-a02fce9643d8 |
NDC | 69367-199 |
Product Type | Human Otc Drug |
Proprietary Name | Doxylamine Succinate and Phenylephrine Hydrochloride |
Generic Name | Doxylamine Succinate And Phenylephrine Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2018-10-25 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | Westminster Pharmaceuticals, LLC |
Substance Name | DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient Strength | 8 mg/1; mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |