STAHIST AD is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Magna Pharmaceuticals, Inc.. The primary component is Chlorcyclizine Hydrochloride; Pseudoephedrine Hydrochloride.
Product ID | 58407-625_330b36a6-17fe-47df-9fd7-d3765f27d904 |
NDC | 58407-625 |
Product Type | Human Otc Drug |
Proprietary Name | STAHIST AD |
Generic Name | Chlorcyclizine Hydrochloride And Pseudoephedrine Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2011-12-20 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | Magna Pharmaceuticals, Inc. |
Substance Name | CHLORCYCLIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
Active Ingredient Strength | 25 mg/1; mg/1 |
Pharm Classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2019-09-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2011-12-20 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-20 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2019-09-01 |
Ingredient | Strength |
---|---|
CHLORCYCLIZINE HYDROCHLORIDE | 25 mg/1 |
SPL SET ID: | ccedbc38-2479-4c35-9f86-a9f29bcfab3f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
58407-624 | Stahist AD | Chlorcyclizine Hydrochloride and Pseudoephedrine Hydrochloride |
58407-625 | STAHIST AD | CHLORCYCLIZINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE |