Lithium Carbonate
- Product NDC
- 53808-0884
- 11-digit product format
- 538080884
- Labeler code
- 53808
- Product ID
- 53808-0884_9d1794d1-822d-4ca7-9cad-6582a965df9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA079139
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 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 |
|---|
| 53808-0884-1 | Lithium Carbonate | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-0884 | LITHIUM CARBONATE CAPSULE [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20141007_e81a731d-433b-4709-b36b-d3463bcfe2e8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53808-0884-1 | 53808088401 | 30 in 1 BLISTER PACK | Historical |