Losartan potassium Tablets, 50 mg
- Product NDC
- 71610-418
- 11-digit product format
- 716100418
- Labeler code
- 71610
- Product ID
- 71610-418_81147c23-9287-4087-8ae7-53731ec9a7ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA201170
- Marketing category
- ANDA
- Marketing start
- 2018-10-23
- 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
- 2021-12-31
- 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 |
|---|
| 71610-418 | LOSARTAN POTASSIUM TABLETS, 25 MG (LOSARTAN POTASSIUM) TABLET LOSARTAN POTASSIUM TABLETS, 50 MG (LOSARTAN POTASSIUM) TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20200508_67828219-e7e2-48f5-9cde-9521e2147222.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-418-45 | 71610041845 | 45 TABLET in 1 BOTTLE (71610-418-45) | 45 tablet | 2020-04-23 | 0000-00-00 | No | No | Current |