Glenmax PEB DM FORTE is a Oral Syrup in the Human Otc Drug category. It is labeled and distributed by Glendale Inc. The primary component is Dextromethorphan Hydrobromide; Phenylephrine Hydrochloride; Brompheniramine Maleate.
Product ID | 70147-223_a072f9ee-7b72-4c8f-81db-9f0b2e022a67 |
NDC | 70147-223 |
Product Type | Human Otc Drug |
Proprietary Name | Glenmax PEB DM FORTE |
Generic Name | Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, And Brompheniramine Maleate |
Dosage Form | Syrup |
Route of Administration | ORAL |
Marketing Start Date | 2015-12-05 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | Glendale Inc |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; BROMPHENIRAMINE MALEATE |
Active Ingredient Strength | 20 mg/5mL; mg/5mL; mg/5mL |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2015-12-05 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC MONOGRAPH FINAL |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | ML |
Marketing Start Date | 2015-12-05 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
DEXTROMETHORPHAN HYDROBROMIDE | 20 mg/5mL |
SPL SET ID: | 441bf71a-042b-48a9-952e-d4dc754d0ae6 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
70147-223 | Glenmax PEB DM FORTE | DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, and BROMPHENIRAMINE MALEATE |
70147-230 | Glenmax PEB DM | DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, and BROMPHENIRAMINE MALEATE |