Duloxetine hydrochloride
- Product NDC
- 70518-1272
- 11-digit product format
- 705181272
- Labeler code
- 70518
- Product ID
- 70518-1272_91287755-2227-c3c8-e053-2995a90ab5d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetin hydrochloride
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090774
- Marketing category
- ANDA
- Marketing start
- 2018-06-20
- Marketing end
- 0000-00-00
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record