escitalopram oxalate
- Product NDC
- 63629-8042
- 11-digit product format
- 636298042
- Labeler code
- 63629
- Product ID
- 63629-8042_d937c069-801a-4359-8ee6-89744c52bd20
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram oxalate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090939
- Marketing category
- ANDA
- Marketing start
- 2012-09-11
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-8042-1 | 63629804201 | 30 TABLET in 1 BOTTLE (63629-8042-1) | 30 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |
| 63629-8042-2 | 63629804202 | 90 TABLET in 1 BOTTLE (63629-8042-2) | 90 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |