Losartan
- Product NDC
- 69543-141
- 11-digit product format
- 695430141
- Labeler code
- 69543
- Product ID
- 69543-141_52f7a69e-4d34-4be4-81ab-8674bd0958e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Virtus Pharmaceuticals
- Application
- ANDA090382
- Marketing category
- ANDA
- Marketing start
- 2015-07-14
- Marketing end
- 2019-05-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0d341e63-aee5-498b-bf9a-b53a43963acf | Product name | 1 | 20260105 |
| de29c5c0-90ba-29da-d7ab-0500274708be | Product name | 6 | 20241009 |
| 15b375b1-89c7-9594-80df-5a8c8864aee0 | Product name | 3 | 20180108 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69543-141-11 | EA - Each | 69543-141 | f4d94f3a-c7a5-4ce0-aacb-c78a722177d2 | 1 | 2015-08-04 |
| 69543-141-30 | EA - Each | 69543-141 | 640dfc12-0b3d-4f73-be55-33483329951b | 1 | 2015-08-04 |
| 69543-141-90 | EA - Each | 69543-141 | bb8c51bb-75c8-49dc-a125-2c920f5b9fca | 1 | 2015-08-04 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 979492 | losartan potassium 50 MG Oral Tablet | PSN | c758fb54-41ac-4cbd-9223-40923c5da800 | 7 |
| 979492 | losartan potassium 50 MG Oral Tablet | SCD | c758fb54-41ac-4cbd-9223-40923c5da800 | 7 |
| 979492 | Losartan K+ 50 MG Oral Tablet | SY | c758fb54-41ac-4cbd-9223-40923c5da800 | 7 |
| 979492 | Losartan Pot 50 MG Oral Tablet | SY | c758fb54-41ac-4cbd-9223-40923c5da800 | 7 |