Losartan Potassium
- Product NDC
- 70518-3305
- 11-digit product format
- 705183305
- Labeler code
- 70518
- Product ID
- 70518-3305_e0dce888-9ae3-007f-e053-2995a90afc3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090428
- Marketing category
- ANDA
- Marketing start
- 2021-12-23
- 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
- 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 |
|---|
| 70518-3305-0 | 70518330500 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3305-0) | 2021-12-23 | 0000-00-00 | No | No | Current |
| 70518-3305-1 | 70518330501 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3305-1) | 2022-06-06 | 0000-00-00 | No | No | Current |