Quetiapine Fumarate
- Product NDC
- 70518-1018
- 11-digit product format
- 705181018
- Labeler code
- 70518
- Product ID
- 70518-1018_e2be746d-b626-5603-e053-2995a90a4f93
- 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
- 2018-02-14
- 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
- 2023-12-31
- 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 |
|---|
| 70518-1018-0 | 70518101800 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1018-0) | 2018-02-14 | 0000-00-00 | No | No | Current |