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 |