Lithium Carbonate
- Product NDC
- 53808-0705
- 11-digit product format
- 538080705
- Labeler code
- 53808
- Product ID
- 53808-0705_fbd9e5c2-570f-4fa1-9ffd-adbf96cb4a5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- NDA017812
- Marketing category
- NDA
- Marketing start
- 2009-07-01
- Marketing end
- 0000-00-00
- Substance
- LITHIUM CARBONATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 53808-0705-1 | Lithium Carbonate | 30 in 1 BLISTER PACK | CAPSULE, GELATIN COATED | 30 | | 2 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| LITHIUM CARBONATE | ACTIVE INGREDIENT | 2BMD2GNA4V | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| LITHIUM CATION | ACTIVE MOIETY | 8H8Z5UER66 | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| FERROSOFERRIC OXIDE | INACTIVE INGREDIENT | XM0M87F357 | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| GELATIN | INACTIVE INGREDIENT | 2G86QN327L | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| POVIDONE K30 | INACTIVE INGREDIENT | U725QWY32X | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| SHELLAC | INACTIVE INGREDIENT | 46N107B71O | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-0705 | LITHIUM CARBONATE CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | Legacy NDC, 1 package rows | 20100324_3318680f-f60c-4c5e-844d-7c6b829ff179.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53808-0705-1 | 53808070501 | 30 in 1 BLISTER PACK | Historical |