QUETIAPINE FUMARATE
- Product NDC
- 71399-4000
- 11-digit product format
- 713994000
- Labeler code
- 71399
- Product ID
- 71399-4000_160c21c2-63f7-49a9-aa10-9767a153cf18
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- QUETIAPINE FUMARATE
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Akron Pharma Inc
- Application
- ANDA209635
- Marketing category
- ANDA
- Marketing start
- 2018-05-10
- Marketing end
- 0000-00-00
- Substance
- QUETIAPINE FUMARATE
- Active strength
- 400 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 |
|---|
| 71399-4000-6 | 71399400006 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71399-4000-6) | 2018-05-10 | 0000-00-00 | No | No | Current |