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NDC 73581-0402-01 MUCUS RELIEF 1200 mg/1 Details
MUCUS RELIEF 1200 mg/1
MUCUS RELIEF is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by YYBA CORP. The primary component is GUAIFENESIN.
MedlinePlus Drug Summary
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: 73581-0402-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
| NDC | 73581-0402 |
|---|---|
| Product ID | 73581-402_0e136ad4-0fa9-8639-e063-6294a90aa9c7 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | MUCUS RELIEF |
| Proprietary Name Suffix | GUAIFENESIN EXTENDED-RELEASE 1200 mg |
| Non-Proprietary Name | GUAIFENESIN |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 1200 |
| Active Ingredient Units | mg/1 |
| Substance Name | GUAIFENESIN |
| Labeler Name | YYBA CORP |
| Pharmaceutical Class | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA213420 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 73581-0402-01 (73581040201)
| NDC Package Code | 73581-402-01 |
|---|---|
| Billing NDC | 73581040201 |
| Package | 100 TABLET in 1 BOTTLE (73581-402-01) |
| Marketing Start Date | 2022-03-02 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |