curist mucus relief maximum strength

Generic: guaifenesin

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

Drug Facts

Product Profile

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

guaifenesin 1200 mg/1

Manufacturer
Little Pharma, Inc.

Identifiers & Regulatory

Product NDC 72559-013
Product ID 72559-013_4c255f1c-c660-024b-e063-6294a90a0a6e
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA213420
Listing Expiration 2027-12-31
Marketing Start 2021-07-23

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 72559013
Hyphenated Format 72559-013

Supplemental Identifiers

RxCUI
310621
UPC
0372559013283
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 curist mucus relief maximum strength (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number ANDA213420 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
source: ndc
Packaging
  • 6 BLISTER PACK in 1 CARTON (72559-013-11) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 150 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-28)
  • 2 BOTTLE in 1 PACKAGE, COMBINATION (72559-013-41) / 150 TABLET, EXTENDED RELEASE in 1 BOTTLE
  • 84 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-64)
source: ndc

Packages (4)

72559-013-11 6 BLISTER PACK in 1 CARTON (72559-013-11) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 72559-013-28 150 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-28) 72559-013-41 2 BOTTLE in 1 PACKAGE, COMBINATION (72559-013-41) / 150 TABLET, EXTENDED RELEASE in 1 BOTTLE 72559-013-64 84 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-64)

Ingredients (1)

guaifenesin (1200 mg/1)

Linked Drug Pages (1)

Curist Mucus Relief Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4c255f1c-c660-024b-e063-6294a90a0a6e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0372559013283"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["c7d1136c-a712-2ac5-e053-2995a90a4dd4"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Little Pharma, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (72559-013-11)  / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "72559-013-11", "marketing_start_date": "20210723"}, {"sample": false, "description": "150 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-28)", "package_ndc": "72559-013-28", "marketing_start_date": "20220406"}, {"sample": false, "description": "2 BOTTLE in 1 PACKAGE, COMBINATION (72559-013-41)  / 150 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "72559-013-41", "marketing_start_date": "20210723"}, {"sample": false, "description": "84 TABLET, EXTENDED RELEASE in 1 BOTTLE (72559-013-64)", "package_ndc": "72559-013-64", "marketing_start_date": "20251115"}], "brand_name": "Curist Mucus Relief Maximum Strength", "product_id": "72559-013_4c255f1c-c660-024b-e063-6294a90a0a6e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "72559-013", "generic_name": "Guaifenesin", "labeler_name": "Little Pharma, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Curist Mucus Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20210723", "listing_expiration_date": "20271231"}