Lithium Carbonate
- Product NDC
- 71335-1543
- 11-digit product format
- 713351543
- Labeler code
- 71335
- Product ID
- 71335-1543_65c3e4f4-c0f2-4ff7-9268-3f566da2116e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate Extended-Release
- 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 |
|---|
| 71335-1543-1 | 71335154301 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1543-1) | 2022-03-10 | 2023-04-30 | No | No | Current |
| 71335-1543-2 | 71335154302 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1543-2) | 2020-03-20 | 2023-04-30 | No | No | Current |
| 71335-1543-3 | 71335154303 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1543-3) | 2022-03-10 | 2023-04-30 | No | No | Current |
| 71335-1543-4 | 71335154304 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1543-4) | 2022-03-10 | 2023-04-30 | No | No | Current |