Losartan Potassium
- Product NDC
- 68645-599
- 11-digit product format
- 686450599
- Labeler code
- 68645
- Product ID
- 68645-599_e5bdda6b-e903-7411-e053-2a95a90a9a37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2014-07-30
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68645-599 | LOSARTAN POTASSIUM TABLET, FILM COATED [LEGACY PHARMACEUTICAL PACKAGING, LLC] | 15 | Legacy NDC | 20241016_e5bddb89-37d3-86d0-e053-2a95a90af4f4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68645-599-54 | 68645059954 | 30 TABLET, FILM COATED in 1 BOTTLE (68645-599-54) | 2022-08-08 | 0000-00-00 | No | No | Current |