Losartan Potassium
- Product NDC
- 53808-0978
- 11-digit product format
- 538080978
- Labeler code
- 53808
- Product ID
- 53808-0978_eb3ec1d7-5abd-466c-b522-43d828bf787b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA090467
- Marketing category
- ANDA
- Marketing start
- 2013-01-01
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 100 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [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 |
|---|
| 53808-0978-1 | Losartan Potassium | 30 in 1 BLISTER PACK | TABLET | 30 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-0978 | LOSARTAN POTASSIUM TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 4 | Legacy NDC, 1 package rows | 20141020_02cdce82-4da9-4c34-89d9-43d542a40261.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53808-0978-1 | 53808097801 | 30 in 1 BLISTER PACK | Historical |