curist mucus relief

Generic: guaifenesin

Labeler: little pharma, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name curist mucus relief
Generic Name guaifenesin
Labeler little pharma, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

guaifenesin 600 mg/1

Manufacturer
Little Pharma, Inc.

Identifiers & Regulatory

Product NDC 72559-017
Product ID 72559-017_2f23e326-e162-2397-e063-6294a90ac4ff
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA213420
Listing Expiration 2026-12-31
Marketing Start 2022-02-21

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 72559017
Hyphenated Format 72559-017

Supplemental Identifiers

RxCUI
636522
UPC
0372559017229
UNII
495W7451VQ
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 curist mucus relief (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA213420 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 200 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-017-22)
  • 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-017-23)
source: ndc

Packages (2)

72559-017-22 200 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-017-22) 72559-017-23 300 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-017-23)

Ingredients (1)

guaifenesin (600 mg/1)

Linked Drug Pages (1)

Curist Mucus Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f23e326-e162-2397-e063-6294a90ac4ff", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0372559017229"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["d8892a82-25a7-552d-e053-2a95a90a72fd"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Little Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-017-22)", "package_ndc": "72559-017-22", "marketing_start_date": "20220221"}, {"sample": false, "description": "300 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-017-23)", "package_ndc": "72559-017-23", "marketing_start_date": "20221017"}], "brand_name": "Curist Mucus Relief", "product_id": "72559-017_2f23e326-e162-2397-e063-6294a90ac4ff", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "72559-017", "generic_name": "Guaifenesin", "labeler_name": "Little Pharma, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Curist Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20220221", "listing_expiration_date": "20261231"}