Duloxetine Hydrochloride
- Product NDC
- 33342-162
- 11-digit product format
- 333420162
- Labeler code
- 33342
- Product ID
- 33342-162_d2bdee38-c510-432f-bf05-a8a573cf459c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Duloxetine Hydrochloride
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Macleods Pharmaceuticals Limited
- Application
- ANDA204815
- Marketing category
- ANDA
- Marketing start
- 2017-03-24
- Substance
- DULOXETINE HYDROCHLORIDE
- Active strength
- 60 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Duloxetine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DULOXETINE HYDROCHLORIDE | 60 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9044SC542W |
| Rxcui | 596926, 596930, 596934 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 33342-162-07 | Duloxetine Hydrochloride | 30 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 30 | | 10 |
| 33342-162-10 | Duloxetine Hydrochloride | 90 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 90 | | 10 |
| 33342-162-12 | Duloxetine Hydrochloride | 10 in 1 CARTON | CAPSULE, DELAYED RELEASE | 10 | | 10 |
| 33342-162-12 | Duloxetine Hydrochloride | 10 in 1 BLISTER PACK | CAPSULE, DELAYED RELEASE | 10 | | 10 |
| 33342-162-44 | Duloxetine Hydrochloride | 1000 in 1 BOTTLE | CAPSULE, DELAYED RELEASE | 1000 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33342-162 | DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE [MACLEODS PHARMACEUTICALS LIMITED] | 9 | Current NDC, Legacy NDC, 5 package rows | 20230926_177ce798-3924-416b-ba37-23dfa911a43b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 33342-162-07 | 33342016207 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-07) | | 2017-03-24 | 0000-00-00 | No | No | Current |
| 33342-162-10 | 33342016210 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-10) | | 2017-03-24 | 0000-00-00 | No | No | Current |
| 33342-162-12 | 33342016212 | 10 BLISTER PACK in 1 CARTON (33342-162-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK | 10 blister pack | 2017-03-24 | 0000-00-00 | No | No | Current |
| 33342-162-44 | 33342016244 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-162-44) | | 2017-03-24 | 0000-00-00 | No | No | Current |