LITHIUM CARBONATE
- Product NDC
- 68788-7716
- 11-digit product format
- 687887716
- Labeler code
- 68788
- Product ID
- 68788-7716_614ae5a5-1974-4b60-af10-00e920dde34a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LITHIUM CARBONATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA079159
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7716-3 | 68788771603 | 30 CAPSULE in 1 BOTTLE (68788-7716-3) | 30 capsule | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7716-6 | 68788771606 | 60 CAPSULE in 1 BOTTLE (68788-7716-6) | 60 capsule | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7716-9 | 68788771609 | 90 CAPSULE in 1 BOTTLE (68788-7716-9) | 90 capsule | 2020-07-01 | 0000-00-00 | No | No | Current |