Lithium Carbonate
- Product NDC
- 50090-3490
- 11-digit product format
- 500903490
- Labeler code
- 50090
- Product ID
- 50090-3490_ab7cb553-b66d-4673-b2d6-ad3e01d3fcb8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA205663
- Marketing category
- ANDA
- Marketing start
- 2017-12-01
- Marketing end
- 0000-00-00
- Substance
- LITHIUM CARBONATE
- Active strength
- 450 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 50090-3490-0 | Lithium Carbonate | 33 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 33 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3490 | LITHIUM CARBONATE TABLET, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 1 package rows | 20180622_2e934815-e452-4ca6-b604-67f89ffed917.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-3490-0 | 50090349000 | 33 in 1 BOTTLE | Historical |