Pill Identifier Duloxetine Hydrochloride - NDC 50771-203
Duloxetine Hydrochloride
Product Code 50771-203
Duloxetine Hydrochloride by Yaopharma Co., Ltd. is a yellow and blue capsule capsule delayed release pellets about 19 mm in size, imprinted with y203;60mg. 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
- TRIETHYL CITRATE
- HYPROMELLOSE 2910 (5 MPA.S)
- HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)
- HYPROMELLOSE 2910 (6 MPA.S)
- FD&C BLUE NO. 1
- FD&C RED NO. 3
- SUCROSE
- TALC
Yaopharma Co., Ltd.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release Pellets
- Yellow (C48330)
- Blue (C48333)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 50771-203-01 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC |
| 50771-203-02 | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
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