Pill Identifier Duloxetine Hydrochloride - NDC 50771-201
Duloxetine Hydrochloride
Product Code 50771-201
Duloxetine Hydrochloride by Yaopharma Co., Ltd. is a yellow capsule capsule delayed release pellets about 14 mm in size, imprinted with y201;20mg. The product is a human prescription drug with active ingredient(s) duloxetine hydrochloride.
Duloxetine Hydrochloride
Active Ingredient(s): Duloxetine Hydrochloride
Inactive Ingredient(s):
- TITANIUM DIOXIDE
- FERRIC OXIDE YELLOW
- STARCH, CORN
- GELATIN
- HYPROMELLOSE 2910 (5 MPA.S)
- HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)
- HYPROMELLOSE 2910 (6 MPA.S)
Yaopharma Co., Ltd.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release Pellets
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
50771-201-01 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC |
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Pill Identification data last updated on: December, 2018
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