Losartan Potassium and Hydrochlorothiazide
- Product NDC
- 60760-472
- 11-digit product format
- 607600472
- Labeler code
- 60760
- Product ID
- 60760-472_7abbdad9-6ae0-300c-e053-2a91aa0a5b65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Losartan Potassium and Hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Marys Medical Park Pharmacy
- Application
- ANDA091629
- Marketing category
- ANDA
- Marketing start
- 2010-10-06
- Marketing end
- 0000-00-00
- Substance
- LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
- Active strength
- 100 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
- 2020-12-31
- 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 |
|---|
| 60760-472-90 | 60760047290 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-472-90) | 2017-12-15 | 0000-00-00 | No | No | Current |