QUETIAPINE FUMARATE
- Product NDC
- 13668-151
- 11-digit product format
- 136680151
- Labeler code
- 13668
- Product ID
- 13668-151_c0dfc06b-dbef-3d69-e053-2995a90aa31d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- QUETIAPINE FUMARATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TORRENT PHARMACEUTICALS LIMITED
- Application
- ANDA200363
- Marketing category
- ANDA
- Marketing start
- 2012-03-27
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13668-151-01 | 13668015101 | 100 TABLET in 1 BOTTLE (13668-151-01) | 100 tablet | 2012-03-27 | 0000-00-00 | No | No | Current |
| 13668-151-05 | 13668015105 | 500 TABLET in 1 BOTTLE (13668-151-05) | 500 tablet | 2012-03-27 | 0000-00-00 | No | No | Current |
| 13668-151-15 | 13668015115 | 1500 TABLET in 1 BOTTLE (13668-151-15) | 1500 tablet | 2012-03-27 | 0000-00-00 | No | No | Current |
| 13668-151-30 | 13668015130 | 30 TABLET in 1 BOTTLE (13668-151-30) | 30 tablet | 2012-03-27 | 0000-00-00 | No | No | Current |
| 13668-151-74 | 13668015174 | 100 TABLET in 1 CARTON (13668-151-74) | 100 tablet | 2012-03-27 | 0000-00-00 | No | No | Current |