Lithium Carbonate
- Product NDC
- 50090-2959
- 11-digit product format
- 500902959
- Labeler code
- 50090
- Product ID
- 50090-2959_43321c58-edd9-4767-adae-c7fa07d5a16c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA017812
- Marketing category
- NDA
- Marketing start
- 1980-11-26
- 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 |
|---|
| 50090-2959-0 | 50090295900 | 32 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2959-0) > 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK | 32 blister pack | 2017-04-06 | 0000-00-00 | No | No | Current |