Lithium Carbonate
- Product NDC
- 63629-1955
- 11-digit product format
- 636291955
- Labeler code
- 63629
- Product ID
- 63629-1955_849ee88c-8e82-4da7-8114-e104f6579f7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate Extended-Release Tablet
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018027
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-12-21
- Marketing end
- 2023-04-30
- Substance
- LITHIUM CARBONATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 63629-1955-1 | 63629195501 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-1955-1) | 2022-03-08 | 2023-04-30 | No | No | Current |