Home NDC 11673-421 up and up mucus relief
Product NDC 11673-421
11-digit product format 116730421
Labeler code 11673
Product ID 11673-421_071469f4-4417-4729-8e75-1536c4dc422f
Type HUMAN OTC DRUG
Nonproprietary name guaifenesin
Dosage form TABLET, MULTILAYER, EXTENDED RELEASE
Route ORAL
Labeler Target Corporation
Application ANDA078912
Marketing category ANDA
Marketing start 2020-07-31
Substance GUAIFENESIN
Active strength 600 mg/1
Pharmacologic classes Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A078912-001 GUAIFENESIN GUAIFENESIN 600MG TABLET, EXTENDED RELEASE / ORAL 2011-11-23 A078912-002 GUAIFENESIN GUAIFENESIN 1.2GM TABLET, EXTENDED RELEASE / ORAL 2020-11-05
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 3 of 3 · 81 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A078912-002 GUAIFENESIN 1.2GM TABLET, EXTENDED RELEASE / ORAL 2020-11-05 a50c72e98297…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base up and up mucus relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GUAIFENESIN 600 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 495W7451VQ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 636522 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-421-01 up and up mucus relief 1 in 1 CARTON TABLET, MULTILAYER, EXTENDED REL 1 5 11673-421-01 up and up mucus relief 20 in 1 BLISTER PACK TABLET, MULTILAYER, EXTENDED REL 20 5 11673-421-60 up and up mucus relief 1 in 1 CARTON TABLET, MULTILAYER, EXTENDED REL 1 5 11673-421-60 up and up mucus relief 20 in 1 BOTTLE TABLET, MULTILAYER, EXTENDED REL 20 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-421 UP AND UP MUCUS RELIEF (GUAIFENESIN) TABLET, MULTILAYER, EXTENDED RELEASE [TARGET CORPORATION] 3 Current NDC, Legacy NDC, 4 package rows 20220601_7c1598f1-1236-48d2-861b-de4715e3f3d2.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 2 · 27 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11673-421-01 11673042101 1 BLISTER PACK in 1 CARTON (11673-421-01) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK 1 blister pack 2025-09-17 No No Current 11673-421-60 11673042160 1 BOTTLE in 1 CARTON (11673-421-60) > 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE 1 bottle 2020-07-31 0000-00-00 No No Current