Lithium Carbonate
- Product NDC
- 50090-6052
- 11-digit product format
- 500906052
- Labeler code
- 50090
- Product ID
- 50090-6052_8ac2ae66-bcdc-417a-a8c5-7070d7acadb2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lithium carbonate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202288
- Marketing category
- ANDA
- Marketing start
- 2012-07-02
- Substance
- LITHIUM CARBONATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lithium Carbonate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LITHIUM CARBONATE | 300 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2BMD2GNA4V |
| Rxcui | 197891 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6052-0 | Lithium Carbonate | 60 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6052 | LITHIUM CARBONATE TABLET, FILM COATED, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231118_baf59ee7-1c98-4f77-96c5-7b50b7acb8f4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-6052-0 | 50090605200 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6052-0) | 2022-08-23 | 0000-00-00 | No | No | Current |