Hydrochlorothiazide
- Product NDC
- 70518-0593
- 11-digit product format
- 705180593
- Labeler code
- 70518
- Product ID
- 70518-0593_8637efe5-5e8b-64bf-e053-2a91aa0a8c2a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078391
- Marketing category
- ANDA
- Marketing start
- 2017-06-27
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- 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