LITHIUM CARBONATE
- Product NDC
- 71335-1067
- 11-digit product format
- 713351067
- Labeler code
- 71335
- Product ID
- 71335-1067_1c207658-0ada-4474-9a98-e54de8381ed5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LITHIUM CARBONATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079159
- Marketing category
- ANDA
- Marketing start
- 2016-12-27
- 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
- 2023-12-31
- 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 |
|---|
| 71335-1067-1 | 71335106701 | 60 CAPSULE in 1 BOTTLE (71335-1067-1) | 60 capsule | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1067-2 | 71335106702 | 100 CAPSULE in 1 BOTTLE (71335-1067-2) | 100 capsule | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1067-3 | 71335106703 | 30 CAPSULE in 1 BOTTLE (71335-1067-3) | 30 capsule | 2019-01-17 | 0000-00-00 | No | No | Current |
| 71335-1067-4 | 71335106704 | 90 CAPSULE in 1 BOTTLE (71335-1067-4) | 90 capsule | 2019-02-06 | 0000-00-00 | No | No | Current |
| 71335-1067-5 | 71335106705 | 120 CAPSULE in 1 BOTTLE (71335-1067-5) | 120 capsule | 2021-12-28 | 0000-00-00 | No | No | Current |