Safetussin DM is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Kramer Laboratories. The primary component is Dextromethorphan Hydrobromide; Guaifenesin.
Product ID | 55505-111_4d8b36ff-ca03-40de-9979-82fcef6056d9 |
NDC | 55505-111 |
Product Type | Human Otc Drug |
Proprietary Name | Safetussin DM |
Generic Name | Dextromethorpan Guaifenesin |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2010-11-29 |
Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
Application Number | part341 |
Labeler Name | Kramer Laboratories |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Active Ingredient Strength | 10 mg/5mL; mg/5mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2017-02-10 |
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 | 2010-11-29 |
Marketing End Date | 2013-08-13 |
Marketing Category | OTC monograph final |
Application Number | part341 |
Product Type | HUMAN OTC DRUG |
Billing Unit | ML |
Marketing Start Date | 2017-02-10 |
Ingredient | Strength |
---|---|
DEXTROMETHORPHAN HYDROBROMIDE | 10 mg/5mL |
SPL SET ID: | ac9f25a7-03cc-461b-af3e-8c16b7146a22 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0295-1111 | Safetussin | Dextromethorpan Guaifenesin |
55505-111 | Safetussin | Dextromethorpan Guaifenesin |
55505-189 | Safetussin | Dextromethorpan Guaifenesin |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SAFETUSSIN 78592800 3068103 Live/Registered |
Kramer Laboratories, Inc. 2005-03-22 |