Sertraline (Page 10 of 10)

Sertraline Tablets USP, 100 mg

Rx only

30 Tablets

NDC 68645-589-54

Sertraline Tablets USP, 100 mg
(click image for full-size original)
SERTRALINE sertraline tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68645-589(NDC:68180-353)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SERTRALINE HYDROCHLORIDE (SERTRALINE) SERTRALINE 100 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
FERRIC OXIDE YELLOW
HYPROMELLOSES
SODIUM STARCH GLYCOLATE TYPE A POTATO
CELLULOSE, MICROCRYSTALLINE
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
MAGNESIUM STEARATE
POLYETHYLENE GLYCOL, UNSPECIFIED
POLYSORBATE 80
TITANIUM DIOXIDE
Product Characteristics
Color YELLOW Score 2 pieces
Shape CAPSULE (capsule shaped, biconvex) Size 13mm
Flavor Imprint Code L;U;D03
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68645-589-54 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077670 02/06/2007 10/31/2022
Labeler — Legacy Pharmaceutical Packaging, LLC (143213275)

Revised: 10/2020 Legacy Pharmaceutical Packaging, LLC

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