mucus d

Generic: guaifenesin, pseudoephedrine hydrochloride

Labeler: cvs woonsocket prescription center, incorporated
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus d
Generic Name guaifenesin, pseudoephedrine hydrochloride
Labeler cvs woonsocket prescription center, incorporated
Dosage Form TABLET, MULTILAYER, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

guaifenesin 1200 mg/1, pseudoephedrine hydrochloride 120 mg/1

Manufacturer
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Identifiers & Regulatory

Product NDC 51316-345
Product ID 51316-345_dfe41906-1124-4258-b68b-0c982b2cca33
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA214407
Listing Expiration 2026-12-31
Marketing Start 2025-04-04

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 51316345
Hyphenated Format 51316-345

Supplemental Identifiers

RxCUI
1244675
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 d (source: ndc)
Generic Name guaifenesin, pseudoephedrine hydrochloride (source: ndc)
Application Number ANDA214407 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
  • 120 mg/1
source: ndc
Packaging
  • 4 BLISTER PACK in 1 CARTON (51316-345-62) / 6 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

51316-345-62 4 BLISTER PACK in 1 CARTON (51316-345-62) / 6 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

guaifenesin (1200 mg/1) pseudoephedrine hydrochloride (120 mg/1)

Linked Drug Pages (1)

mucus d ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dfe41906-1124-4258-b68b-0c982b2cca33", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "6V9V2RYJ8N"], "rxcui": ["1244675"], "spl_set_id": ["c8026a56-4249-48de-b763-2d1c55731733"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (51316-345-62)  / 6 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "51316-345-62", "marketing_start_date": "20250404"}], "brand_name": "mucus d", "product_id": "51316-345_dfe41906-1124-4258-b68b-0c982b2cca33", "dosage_form": "TABLET, MULTILAYER, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "51316-345", "generic_name": "guaifenesin, pseudoephedrine hydrochloride", "labeler_name": "CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "mucus d", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA214407", "marketing_category": "ANDA", "marketing_start_date": "20250404", "listing_expiration_date": "20261231"}