Losartan Potassium
- Product NDC
- 70518-1858
- 11-digit product format
- 705181858
- Labeler code
- 70518
- Product ID
- 70518-1858_e3a0ee95-b4a1-6caf-e053-2a95a90ad210
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091497
- Marketing category
- ANDA
- Marketing start
- 2019-02-07
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1858 | LOSARTAN POTASSIUM TABLET, FILM COATED [REMEDYREPACK INC.] | 8 | Legacy NDC | 20250302_2983208f-370b-48c4-bcbe-83235fb87ff9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1858-1 | 70518185801 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1858-1) | 2022-07-12 | 0000-00-00 | No | No | Current |