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NDC 46122-0420-03 Mucus DM 60; 1200 mg/1; mg/1 Details
Mucus DM 60; 1200 mg/1; mg/1
Mucus DM is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Amerisource Bergen. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.
MedlinePlus Drug Summary
Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.
Related Packages: 46122-0420-03Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Dextromethorphan
Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
Related Packages: 46122-0420-03Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
NDC | 46122-0420 |
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Product ID | 46122-420_59ff2a9d-3180-41b5-9a63-98ae793a8a0f |
Associated GPIs | 43997002527475 |
GCN Sequence Number | 042105 |
GCN Sequence Number Description | guaifenesin/dextromethorphan TAB ER 12H 1200-60MG ORAL |
HIC3 | B3T |
HIC3 Description | NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION |
GCN | 93677 |
HICL Sequence Number | 000223 |
HICL Sequence Number Description | GUAIFENESIN/DEXTROMETHORPHAN HBR |
Brand/Generic | Generic |
Proprietary Name | Mucus DM |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Guaifenesin and Dextromethorphan HBr |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, EXTENDED RELEASE |
Route | ORAL |
Active Ingredient Strength | 60; 1200 |
Active Ingredient Units | mg/1; mg/1 |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Labeler Name | Amerisource Bergen |
Pharmaceutical Class | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Ant |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA206941 |
Listing Certified Through | 2024-12-31 |
Package
NDC 46122-0420-03 (46122042003)
NDC Package Code | 46122-420-03 |
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Billing NDC | 46122042003 |
Package | 4 BLISTER PACK in 1 CARTON (46122-420-03) / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Marketing Start Date | 2017-03-17 |
NDC Exclude Flag | N |
Pricing Information | N/A |