Quetiapine Fumarate
- Product NDC
- 50090-3392
- 11-digit product format
- 500903392
- Labeler code
- 50090
- Product ID
- 50090-3392_4c8afdc5-a4cd-4f3a-b9db-562ca4654cad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine Fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202674
- Marketing category
- ANDA
- Marketing start
- 2016-07-01
- Marketing end
- 0000-00-00
- Substance
- QUETIAPINE FUMARATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50090-3392-0 | 50090339200 | 33 TABLET, FILM COATED in 1 BOTTLE (50090-3392-0) | 2018-03-08 | 0000-00-00 | No | No | Current |