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NDC 60687-0651-21 Mucinex DM 30; 600 mg/1; mg/1 Details
Mucinex DM 30; 600 mg/1; mg/1
Mucinex DM is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by American Health Packaging. 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: 60687-0651-21Last Updated: 12/01/2022
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: 60687-0651-21Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
| NDC | 60687-0651 |
|---|---|
| Product ID | 60687-651_025765c9-619a-7e54-e063-6394a90afde3 |
| Associated GPIs | |
| GCN Sequence Number | 012074 |
| GCN Sequence Number Description | guaifenesin/dextromethorphan TAB ER 12H 600MG-30MG ORAL |
| HIC3 | B3T |
| HIC3 Description | NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION |
| GCN | 53550 |
| HICL Sequence Number | 000223 |
| HICL Sequence Number Description | GUAIFENESIN/DEXTROMETHORPHAN HBR |
| Brand/Generic | Brand |
| Proprietary Name | Mucinex DM |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Guaifenesin and Dextromethorphan Hydrobromide |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 30; 600 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Labeler Name | American Health Packaging |
| 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 | NDA |
| Application Number | NDA021620 |
| Listing Certified Through | n/a |
Package
NDC 60687-0651-21 (60687065121)
| NDC Package Code | 60687-651-21 |
|---|---|
| Billing NDC | 60687065121 |
| Package | 30 BLISTER PACK in 1 CARTON (60687-651-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-651-11) |
| Marketing Start Date | 2022-07-14 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 0.60811 |
| Pricing Unit | EA |
| Effective Date | 2023-12-20 |
| NDC Description | MUCINEX DM ER 600-30 MG TABLET |
| Pharmacy Type Indicator | C/I |
| OTC | Y |
| Explanation Code | 2 |
| Classification for Rate Setting | B |
| As of Date | 2024-02-21 |