Quetiapine
- Product NDC
- 63629-2479
- 11-digit product format
- 636292479
- Labeler code
- 63629
- Product ID
- 63629-2479_c58052a5-f976-42b2-899d-fedea696edd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209635
- Marketing category
- ANDA
- Marketing start
- 2017-11-29
- Marketing end
- 0000-00-00
- Substance
- QUETIAPINE FUMARATE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2479-1 | 63629247901 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2479-1) | 2021-03-08 | 0000-00-00 | No | No | Current |