382 382 (Duloxetine Hydrochloride Delayed-Release 30 mg)
Pill with imprint 382 382 is Blue & White, Capsule-shape and has been identified as Duloxetine Hydrochloride Delayed-Release 30 mg. It is supplied by Sun Pharma Global FZE.
Duloxetine is used in the treatment of chronic pain; back pain; anxiety; depression; diabetic peripheral neuropathy and belongs to the drug class serotonin-norepinephrine reuptake inhibitors. Risk cannot be ruled out during pregnancy. Duloxetine 30 mg is not a controlled substance under the Controlled Substances Act (CSA).
Images for 382 382
Duloxetine Hydrochloride Delayed-Release
- Imprint
- 382 382
- Strength
- 30 mg
- Color
- Blue & White
- Shape
- Capsule-shape
- Availability
- Prescription only
- Drug Class
- Serotonin-norepinephrine reuptake inhibitors
- Pregnancy Category
- C - Risk cannot be ruled out
- CSA Schedule
- Not a controlled drug
- Labeler / Supplier
- Sun Pharma Global FZE
- National Drug Code (NDC)
- 47335-0382
- Inactive Ingredients
-
sucrose,
hypromelloses,
mannitol,
magnesium silicate,
methacrylic acid - ethyl acrylate copolymer (1:1) type a,
triethyl citrate,
sodium hydroxide,
gelatin,
sodium lauryl sulfate,
titanium dioxide,
FD&C Blue No. 2,
shellac,
alcohol,
isopropyl alcohol,
butyl alcohol,
propylene glycol,
ammonia,
ferrosoferric oxide,
potassium hydroxide,
water,
corn starch
Note: Inactive ingredients may vary.
Related images for "382 382"
More about duloxetine
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- Drug class: serotonin-norepinephrine reuptake inhibitors
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