Quetiapine Fumarate
- Product NDC
- 70518-0989
- 11-digit product format
- 705180989
- Labeler code
- 70518
- Product ID
- 70518-0989_8f80cea2-6d9c-f024-e053-2a95a90a6c63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine Fumarate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202674
- Marketing category
- ANDA
- Marketing start
- 2018-01-25
- 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