Losartan Potassium
- Product NDC
- 0615-8208
- 11-digit product format
- 006158208
- Labeler code
- 0615
- Product ID
- 0615-8208_4b1f2d99-a521-46c1-a96e-b66ceef54687
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA090467
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 2021-05-31
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8208-05 | 00615820805 | 15 TABLET in 1 BLISTER PACK (0615-8208-05) | 15 tablet | 2018-04-03 | 2021-05-31 | No | No | Current |
| 0615-8208-30 | 00615820830 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8208-30) > 5 TABLET in 1 BLISTER PACK | 6 blister pack | 2018-04-10 | 2021-05-31 | No | No | Current |
| 0615-8208-39 | 00615820839 | 30 TABLET in 1 BLISTER PACK (0615-8208-39) | 30 tablet | 2018-04-03 | 2021-05-31 | No | No | Current |