Losartan potassium
- Product NDC
- 43063-483
- 11-digit product format
- 430630483
- Labeler code
- 43063
- Product ID
- 43063-483_d2a9d8bd-9e6e-da68-e053-2a95a90a2336
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA077424
- 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
- 2022-12-31
- 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 |
|---|
| 43063-483-30 | 43063048330 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-483-30) | 2015-10-23 | 0000-00-00 | No | No | Current |