Indapamide
- Product NDC
- 70518-1324
- 11-digit product format
- 705181324
- Labeler code
- 70518
- Product ID
- 70518-1324_92429d8f-6871-9e76-e053-2995a90a6be9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Indapamide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074722
- Marketing category
- ANDA
- Marketing start
- 2018-07-26
- Marketing end
- 0000-00-00
- Substance
- INDAPAMIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record