Quetiapine Fumarate
- Product NDC
- 70518-0974
- 11-digit product format
- 705180974
- Labeler code
- 70518
- Product ID
- 70518-0974_e2ac19ce-2c17-26a8-e053-2a95a90a9d52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine Fumarate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201504
- Marketing category
- ANDA
- Marketing start
- 2018-01-22
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-0974-0 | 70518097400 | 30 TABLET in 1 BLISTER PACK (70518-0974-0) | 30 tablet | 2018-01-22 | 0000-00-00 | No | No | Current |
| 70518-0974-1 | 70518097401 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-0974-1) | 30 tablet | 2018-05-09 | 0000-00-00 | No | No | Current |