Lithium Carbonate
- Product NDC
- 63629-8282
- 11-digit product format
- 636298282
- Labeler code
- 63629
- Product ID
- 63629-8282_3020f1c5-18f0-4b23-b0d1-f568707b2f52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204779
- Marketing category
- ANDA
- Marketing start
- 2016-03-23
- Marketing end
- 0000-00-00
- Substance
- LITHIUM CARBONATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-8282-1 | 63629828201 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8282-1) | 2020-10-15 | 0000-00-00 | No | No | Current |
| 63629-8282-2 | 63629828202 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8282-2) | 2019-12-06 | 0000-00-00 | No | No | Current |
| 63629-8282-3 | 63629828203 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8282-3) | 2019-12-06 | 0000-00-00 | No | No | Current |
| 63629-8282-4 | 63629828204 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8282-4) | 2020-03-03 | 0000-00-00 | No | No | Current |