Losartan Potassium
- Product NDC
- 50090-6044
- 11-digit product format
- 500906044
- Labeler code
- 50090
- Product ID
- 50090-6044_ec0e6ce6-29ca-47b0-86a4-843778b9a857
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2014-07-30
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6044 | LOSARTAN POTASSIUM TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC | 20231122_475dfb20-354c-46b0-8520-dd36f21e17c6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-6044-0 | 50090604400 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6044-0) | 2022-07-15 | 0000-00-00 | No | No | Current |
| 50090-6044-1 | 50090604401 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-6044-1) | 2022-07-15 | 0000-00-00 | No | No | Current |