Losartan Potassium
- Product NDC
- 53002-3643
- 11-digit product format
- 530023643
- Labeler code
- 53002
- Product ID
- 53002-3643_ee2beb1d-0269-48e2-9674-8d1fcb019ed2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA090083
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 53002-3643-0 | 53002364300 | 100 TABLET, FILM COATED in 1 BOTTLE (53002-3643-0) | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-3643-3 | 53002364303 | 30 TABLET, FILM COATED in 1 BOTTLE (53002-3643-3) | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-3643-9 | 53002364309 | 90 TABLET, FILM COATED in 1 BOTTLE (53002-3643-9) | 2019-01-01 | 0000-00-00 | No | No | Current |