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United States · US · US:71335-2642_bfd50410-1289-4b5d-86df-3b939d50bc27

Mucus Relief

Orange BookUNIISPLATC R05CA03

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeR05CA03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    7133526421
    30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-1)
  • ndc11
    7133526422
    20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-2)
  • ndc11
    7133526423
    60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-3)
  • ndc11
    7133526424
    40 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-4)
  • ndc11
    7133526425
    14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-5)
  • ndc11
    7133526426
    6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2642-6)

Annotations

UNII (FDA Substance ID)
495W7451VQ
GUAIFENESIN
RxCUI 5032
Orange Book
A209215
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": "71335-2642_bfd50410-1289-4b5d-86df-3b939d50bc27",
  "productndc": "71335-2642",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "209215",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "600MG",
        "product_no": "001",
        "approval_date": "Sep 6, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "1.2GM",
        "product_no": "002",
        "approval_date": "Sep 6, 2017"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "GUAIFENESIN",
  "proprietary_name": "Mucus Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA209215",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Guaifenesin",
  "start_marketing_date": "20190923",
  "active_numerator_strength": "600"
}

Related drugs

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