mucus relief d (0536-1137)

Drug Facts

Product Profile

Brand Name mucus relief d

Generic Name guaifenesin and pseudoephedrine hydrochloride

Labeler rugby laboratories

Dosage Form TABLET, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

guaifenesin 600 mg/1, pseudoephedrine hydrochloride 60 mg/1

Manufacturer

Rugby Laboratories

Identifiers & Regulatory

Product NDC 0536-1137

Product ID 0536-1137_a0c55dff-f90c-4af5-ac04-6f09bbcb5827

Product Type HUMAN OTC DRUG

Marketing Category NDA

Application Number NDA021585

Listing Expiration 2026-12-31

Marketing Start 2018-03-01

Pharmacologic Class

Established (EPC)

expectorant [epc]

Physiologic Effect

decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05361137

Hyphenated Format 0536-1137

Supplemental Identifiers

RxCUI

1305603

UNII

495W7451VQ 6V9V2RYJ8N

NUI

N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name mucus relief d (source: ndc)

Generic Name guaifenesin and pseudoephedrine hydrochloride (source: ndc)

Application Number NDA021585 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

600 mg/1
60 mg/1

source: ndc

Packaging

1 BLISTER PACK in 1 CARTON (0536-1137-21) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
2 BLISTER PACK in 1 CARTON (0536-1137-36) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

source: ndc

Packages (2)

0536-1137-21 1 BLISTER PACK in 1 CARTON (0536-1137-21) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 0536-1137-36 2 BLISTER PACK in 1 CARTON (0536-1137-36) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

guaifenesin (600 mg/1) pseudoephedrine hydrochloride (60 mg/1)

Linked Drug Pages (1)

Mucus Relief D ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "a0c55dff-f90c-4af5-ac04-6f09bbcb5827", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "6V9V2RYJ8N"], "rxcui": ["1305603"], "spl_set_id": ["f043ec98-6eb4-4c0c-b74c-56fdd867a520"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rugby Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0536-1137-21)  / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0536-1137-21", "marketing_start_date": "20180301"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0536-1137-36)  / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "0536-1137-36", "marketing_start_date": "20180301"}], "brand_name": "Mucus Relief D", "product_id": "0536-1137_a0c55dff-f90c-4af5-ac04-6f09bbcb5827", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0536-1137", "generic_name": "Guaifenesin and Pseudoephedrine Hydrochloride", "labeler_name": "Rugby Laboratories", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief D", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "NDA021585", "marketing_category": "NDA", "marketing_start_date": "20180301", "listing_expiration_date": "20261231"}