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 |