Bronkaid Dual Action Formula is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Foundation Consumer Healthcare Llc. The primary component is Ephedrine Sulfate; Guaifenesin.
Product ID | 69536-425_4528a201-937a-4c81-be74-d8fc89733243 |
NDC | 69536-425 |
Product Type | Human Otc Drug |
Proprietary Name | Bronkaid Dual Action Formula |
Generic Name | Ephedrine Sulfate And Guaifenesin |
Dosage Form | Tablet, Coated |
Route of Administration | ORAL |
Marketing Start Date | 2006-01-01 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | Foundation Consumer Healthcare LLC |
Substance Name | EPHEDRINE SULFATE; GUAIFENESIN |
Active Ingredient Strength | 25 mg/1; mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2006-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-01-01 |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-01-01 |
Ingredient | Strength |
---|---|
EPHEDRINE SULFATE | 25 mg/1 |
SPL SET ID: | a7a2351e-f03f-442c-872c-1bec67ebf333 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BRONKAID 72202920 0788673 Live/Registered |
DREW PHARMACAL CO., INC. 1964-09-29 |