Losartan Potassium
- Product NDC
- 50090-2882
- 11-digit product format
- 500902882
- Labeler code
- 50090
- Product ID
- 50090-2882_43a82a79-ff05-42d6-b9f1-1f1997b59ead
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM
- Active strength
- 50 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-2882-0 | Losartan Potassium | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 36 |
| 50090-2882-1 | Losartan Potassium | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 36 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2882 | LOSARTAN POTASSIUM TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 34 | Legacy NDC, 2 package rows | 20240206_73bb1210-fa46-4c88-b07c-14ff5580ef18.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 |
|---|
| 50090-2882-0 | 50090288200 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-2882-0) | 2017-04-26 | 0000-00-00 | No | No | Current |
| 50090-2882-1 | 50090288201 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-2882-1) | 2017-02-22 | 0000-00-00 | No | No | Current |