atomoxetine
- Product NDC
- 65841-608
- 11-digit product format
- 658410608
- Labeler code
- 65841
- Product ID
- 65841-608_b4182f27-7ee6-4429-91cc-2dca5d97a119
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atomoxetine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA079017
- Marketing category
- ANDA
- Marketing start
- 2017-12-06
- Marketing end
- 0000-00-00
- Substance
- ATOMOXETINE HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Norepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 65841-608-02 | 65841060802 | 2000 CAPSULE in 1 BOTTLE (65841-608-02) | 2000 capsule | 2017-12-06 | 0000-00-00 | No | No | Current |
| 65841-608-06 | 65841060806 | 30 CAPSULE in 1 BOTTLE (65841-608-06) | 30 capsule | 2017-12-06 | 0000-00-00 | No | No | Current |
| 65841-608-10 | 65841060810 | 1000 CAPSULE in 1 BOTTLE (65841-608-10) | 1000 capsule | 2017-12-06 | 0000-00-00 | No | No | Current |
| 65841-608-14 | 65841060814 | 60 CAPSULE in 1 BOTTLE (65841-608-14) | 60 capsule | 2017-12-06 | 0000-00-00 | No | No | Current |
| 65841-608-16 | 65841060816 | 90 CAPSULE in 1 BOTTLE (65841-608-16) | 90 capsule | 2017-12-06 | 0000-00-00 | No | No | Current |
| 65841-608-77 | 65841060877 | 10 BLISTER PACK in 1 CARTON (65841-608-77) > 10 CAPSULE in 1 BLISTER PACK (65841-608-30) | 10 blister pack | 2017-12-06 | 0000-00-00 | No | No | Current |