Atomoxetine
- Product NDC
- 66993-044
- 11-digit product format
- 669930044
- Labeler code
- 66993
- Product ID
- 66993-044_c4159827-82b0-4cea-a1a0-b86403780f88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atomoxetine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA021411
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-05-30
- Marketing end
- 2022-03-31
- Substance
- ATOMOXETINE HYDROCHLORIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-044-30 | 66993004430 | 30 CAPSULE in 1 BOTTLE (66993-044-30) | 30 capsule | 2017-05-30 | 0000-00-00 | No | No | Current |