LOSARTAN POTASSIUM
- Product NDC
- 50090-4252
- 11-digit product format
- 500904252
- Labeler code
- 50090
- Product ID
- 50090-4252_6e81770a-6a92-4c46-82f3-8fb3554ad377
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091541
- Marketing category
- ANDA
- Marketing start
- 2012-12-06
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 25 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4252-0 | LOSARTAN POTASSIUM | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
| 50090-4252-1 | LOSARTAN POTASSIUM | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4252 | LOSARTAN POTASSIUM TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 4 | Legacy NDC, 2 package rows | 20200225_d142e482-e562-48f1-b164-e8980eadb0b3.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 |
|---|
| 50090-4252-0 | 50090425200 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-4252-0) | 2019-04-05 | 0000-00-00 | No | No | Current |
| 50090-4252-1 | 50090425201 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4252-1) | 2019-04-04 | 0000-00-00 | No | No | Current |