Losartan Potassium
- Product NDC
- 43063-881
- 11-digit product format
- 430630881
- Labeler code
- 43063
- Product ID
- 43063-881_e0f264a0-69ee-3060-e053-2a95a90a1e4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA090467
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-881-30 | 43063088130 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-881-30) | 30 tablet | 2018-08-14 | 0000-00-00 | No | No | Current |