Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 70518-0786
- 11-digit product format
- 705180786
- Labeler code
- 70518
- Product ID
- 70518-0786_e235b863-5ea1-6fa4-e053-2995a90aaeef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091617
- Marketing category
- ANDA
- Marketing start
- 2017-10-12
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
- Active strength
- 25 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0786-1 | 70518078601 | 30 POUCH in 1 BOX (70518-0786-1) > 1 TABLET, FILM COATED in 1 POUCH (70518-0786-2) | 30 pouch | 2022-03-10 | 0000-00-00 | No | No | Current |