Duloxetine
- Product NDC
- 71205-602
- 11-digit product format
- 712050602
- Labeler code
- 71205
- Product ID
- 71205-602_f73fb658-ff2c-4847-a1ee-e551d2776f52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA208706
- Marketing category
- ANDA
- Marketing start
- 2017-03-16
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9044SC542W | DULOXETINE HYDROCHLORIDE | 136434-34-9 | DULOXETINE HYDROCHLORIDE |
| O5TNM5N07U | DULOXETINE | 116539-59-4 | Duloxetine |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-602-30 | 71205060230 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-30) | 2021-08-20 | No | No | Historical |
| 71205-602-60 | 71205060260 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-60) | 2021-08-20 | No | No | Historical |
| 71205-602-90 | 71205060290 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90) | 2021-08-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Duloxetine | Proficient Rx LP | 2022-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |