Losartan Potassium
- Product NDC
- 63187-391
- 11-digit product format
- 631870391
- Labeler code
- 63187
- Product ID
- 63187-391_a9de2bb4-1409-4daf-acd1-e3a54b03d41b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA090467
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-391 | LOSARTAN POTASSIUM TABLET [PROFICIENT RX LP] | 3 | Legacy NDC | 20210115_857945c0-0ba7-4d0d-ab42-e6087b40fb5b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-391-30 | 63187039130 | 30 TABLET in 1 BOTTLE (63187-391-30) | 30 tablet | 2016-12-01 | 0000-00-00 | No | No | Current |
| 63187-391-60 | 63187039160 | 60 TABLET in 1 BOTTLE (63187-391-60) | 60 tablet | 2016-12-01 | 0000-00-00 | No | No | Current |
| 63187-391-90 | 63187039190 | 90 TABLET in 1 BOTTLE (63187-391-90) | 90 tablet | 2016-12-01 | 0000-00-00 | No | No | Current |