Quetiapine
- Product NDC
- 50090-2830
- 11-digit product format
- 500902830
- Labeler code
- 50090
- Product ID
- 50090-2830_f73a239b-9cd0-4b61-b4c2-f3c67cd6b040
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quetiapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202152
- Marketing category
- ANDA
- Marketing start
- 2015-12-01
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2830-0 | 50090283000 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2830-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 33 blister pack | 2017-02-01 | 0000-00-00 | No | No | Current |