Losortan Potassium
- Product NDC
- 43063-347
- 11-digit product format
- 430630347
- Labeler code
- 43063
- Product ID
- 43063-347_db71e8f3-4e9d-0cf8-e053-2995a90a35dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078243
- Marketing category
- ANDA
- Marketing start
- 2010-10-04
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-347-30 | 43063034730 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-347-30) | 2012-01-13 | 0000-00-00 | No | No | Current |