Lithium Carbonate
- Product NDC
- 50090-3918
- 11-digit product format
- 500903918
- Labeler code
- 50090
- Product ID
- 50090-3918_6d9aae46-eba3-43cb-ad02-c33b765b37b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lithium carbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090702
- Marketing category
- ANDA
- Marketing start
- 2009-12-15
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3918-0 | Lithium Carbonate | 32 in 1 BOTTLE | CAPSULE | 32 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3918 | LITHIUM CARBONATE CAPSULE [A-S MEDICATION SOLUTIONS] | 5 | Legacy NDC, 1 package rows | 20200122_d5593458-5965-48ad-9086-96f8651938dc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3918-0 | 50090391800 | 32 CAPSULE in 1 BOTTLE (50090-3918-0) | 32 capsule | 2018-12-06 | 0000-00-00 | No | No | Current |