LOSARTAN POTASSIUM
- Product NDC
- 50090-4048
- 11-digit product format
- 500904048
- Labeler code
- 50090
- Product ID
- 50090-4048_0da22b0f-b7f8-457f-a75d-a9dfcbbb41ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LOSARTAN POTASSIUM
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090382
- Marketing category
- ANDA
- Marketing start
- 2018-01-04
- 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
- 2020-12-31
- 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 |
|---|
| 50090-4048-0 | LOSARTAN POTASSIUM100 mg | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
| 50090-4048-1 | LOSARTAN POTASSIUM100 mg | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4048 | LOSARTAN POTASSIUM 100 MG (LOSARTAN POTASSIUM) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20190501_b5b9d674-4b53-459c-8322-f2ac1ce7810e.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 |
|---|
| 50090-4048-0 | 50090404800 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4048-0) | 2019-01-11 | 0000-00-00 | No | No | Current |
| 50090-4048-1 | 50090404801 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-4048-1) | 2018-01-04 | 0000-00-00 | No | No | Current |