Atomoxetine
- Product NDC
- 66993-041
- 11-digit product format
- 669930041
- Labeler code
- 66993
- Product ID
- 66993-041_76c50d5c-813c-4388-bb3e-8a7a6f6a6a24
- 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
- 0000-00-00
- Substance
- ATOMOXETINE HYDROCHLORIDE
- Active strength
- 18 mg/1
- Pharmacologic classes
- Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 66993-041-30 | 66993004130 | 30 CAPSULE in 1 BOTTLE (66993-041-30) | 30 capsule | 2017-05-30 | 0000-00-00 | No | No | Current |