quetiapine fumarate
- Product NDC
- 70518-1029
- 11-digit product format
- 705181029
- Labeler code
- 70518
- Product ID
- 70518-1029_8fe9164b-8f4e-7a3c-e053-2a95a90a9ebe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- quetiapine fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090960
- Marketing category
- ANDA
- Marketing start
- 2018-02-21
- Marketing end
- 0000-00-00
- Substance
- QUETIAPINE FUMARATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Atypical Antipsychotic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record