mucus relief

Generic: guaifenesin

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler p & l development, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

guaifenesin 1200 mg/1

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-237
Product ID 59726-237_885e0a80-bf98-4f71-a04f-1e94a30a8362
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Listing Expiration 2026-12-31
Marketing Start 2025-02-15

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 59726237
Hyphenated Format 59726-237

Supplemental Identifiers

RxCUI
310621
UPC
0359726157070
UNII
495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

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 (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA207342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
source: ndc
Packaging
  • 7 BLISTER PACK in 1 CARTON (59726-237-07) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 14 BLISTER PACK in 1 CARTON (59726-237-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

59726-237-07 7 BLISTER PACK in 1 CARTON (59726-237-07) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 59726-237-14 14 BLISTER PACK in 1 CARTON (59726-237-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (1)

guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Mucus Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "885e0a80-bf98-4f71-a04f-1e94a30a8362", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0359726157070"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["a2d14780-4a69-496e-86fe-7f2443cb0f20"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["P & L Development, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "7 BLISTER PACK in 1 CARTON (59726-237-07)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "59726-237-07", "marketing_start_date": "20250215"}, {"sample": false, "description": "14 BLISTER PACK in 1 CARTON (59726-237-14)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "59726-237-14", "marketing_start_date": "20250215"}], "brand_name": "Mucus Relief", "product_id": "59726-237_885e0a80-bf98-4f71-a04f-1e94a30a8362", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "59726-237", "generic_name": "Guaifenesin", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20250215", "listing_expiration_date": "20261231"}