NDCFind

Guaifenesin 82804-0265

Product NDC

82804-0265
Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Otc Drug
Marketing Start
August 19, 2022
Listing Expires
December 31, 2027
Application
ANDA213420

Active Ingredients

IngredientStrength
Guaifenesin600 mg/1

Drug Class

Expectorant [EPC]Decreased Respiratory Secretion Viscosity [PE]Expectorant [EPC]

Packaging Options(1)

20 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-265-20)