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United States · US · US:79481-0709_76b7080f-c2e7-4b3a-b545-029330591125
Mucus D
Orange BookUNIISPLATC R05CA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMeijer, Inc.
CountryUS (United States)
ATC codeR05CA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1179481070911 BLISTER PACK in 1 CARTON (79481-0709-1) / 18 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
495W7451VQ
GUAIFENESIN
RxCUI 5032
Orange Book
A214407
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "495W7451VQ",
"rxcui": "5032",
"inchikey": "HSRJKNPTNIJEKV-UHFFFAOYSA-N",
"display_name": "GUAIFENESIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"84b5d83d-aea5-42ed-b20c-96d3b389c8c0": {
"match": "brand_token",
"title": "MUCUS RELIEF DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) TABLET, EXTENDED RELEASE [RITE AID CORPORATION]",
"spl_version": "3",
"published_date": "2026-05-28"
}
},
"productid": "79481-0709_76b7080f-c2e7-4b3a-b545-029330591125",
"productndc": "79481-0709",
"dosage_form": "TABLET, MULTILAYER, EXTENDED RELEASE",
"orange_book": {
"appl_no": "214407",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "600MG;60MG",
"product_no": "001",
"approval_date": "Feb 1, 2022"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "1.2GM;120MG",
"product_no": "002",
"approval_date": "Feb 1, 2022"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE",
"proprietary_name": "Mucus D",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA214407",
"marketing_category": "ANDA",
"nonproprietary_name": "guaifenesin and pseudoephedrine hydrochloride",
"start_marketing_date": "20250107",
"active_numerator_strength": "600; 60"
}Related drugs
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