Quetiapine fumarate
- Product NDC
- 70518-0556
- 11-digit product format
- 705180556
- Labeler code
- 70518
- Product ID
- 70518-0556_85b76860-a1f7-19a3-e053-2991aa0a1b39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201190
- Marketing category
- ANDA
- Marketing start
- 2017-05-25
- 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