FDA.reportPublic FDA data

Guaifenesin and Dextromethorphan HBr

Product NDC
51660-110
11-digit product format
516600110
Labeler code
51660
Product ID
51660-110_4fe442c3-cd08-b83f-e063-6294a90a9411
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin and Dextromethorphan HBr
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
OHM LABORATORIES INC
Application
ANDA214781
Marketing category
ANDA
Marketing start
2021-07-01
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
60; 1200 mg/1; mg/1
Pharmacologic classes
Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Guaifenesin and Dextromethorphan HBr
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DEXTROMETHORPHAN HYDROBROMIDE60 mg/1
GUAIFENESIN1200 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9D2RTI9KYH, 495W7451VQ
Rxcui1099074

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212
76633df9-0d59-4b88-03ed-21dee1b966f8Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51660-110-54Guaifenesin and Dextromethorphan HBr14 in 1 BLISTER PACKTABLET, EXTENDED RELEASE145
51660-110-54Guaifenesin and Dextromethorphan HBr1 in 1 CARTONTABLET, EXTENDED RELEASE15
51660-110-58Guaifenesin and Dextromethorphan HBr14 in 1 BLISTER PACKTABLET, EXTENDED RELEASE145
51660-110-58Guaifenesin and Dextromethorphan HBr3 in 1 CARTONTABLET, EXTENDED RELEASE35
51660-110-86Guaifenesin and Dextromethorphan HBr14 in 1 BLISTER PACKTABLET, EXTENDED RELEASE145
51660-110-86Guaifenesin and Dextromethorphan HBr2 in 1 CARTONTABLET, EXTENDED RELEASE25

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51660-110GUAIFENESIN AND DEXTROMETHORPHAN HBR TABLET, EXTENDED RELEASE [OHM LABORATORIES INC]3Current NDC, Legacy NDC, 6 package rows20210903_07b9854d-1ec6-4c8a-983e-96ed1e2de1c2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1099074guaiFENesin 1200 MG / dextromethorphan HBr 60 MG 12HR Extended Release Oral TabletPSN07b9854d-1ec6-4c8a-983e-96ed1e2de1c25
109907412 HR dextromethorphan hydrobromide 60 MG / guaifenesin 1200 MG Extended Release Oral TabletSCD07b9854d-1ec6-4c8a-983e-96ed1e2de1c25
1099074dextromethorphan hydrobromide 60 MG / guaifenesin 1200 MG 12 HR Extended Release Oral TabletSY07b9854d-1ec6-4c8a-983e-96ed1e2de1c25

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51660-110-54516600110541 BLISTER PACK in 1 CARTON (51660-110-54) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK1 blister pack2021-07-010000-00-00NoNoCurrent
51660-110-58516600110583 BLISTER PACK in 1 CARTON (51660-110-58) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK3 blister pack2026-06-050Current
51660-110-86516600110862 BLISTER PACK in 1 CARTON (51660-110-86) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK2 blister pack2021-07-010000-00-00NoNoCurrent