INDAPAMIDE
- Product NDC
- 43975-217
- 11-digit product format
- 439750217
- Labeler code
- 43975
- Product ID
- 43975-217_474ce187-facf-4755-9c22-397c5ed29837
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- INDAPAMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA075201
- Marketing category
- ANDA
- Marketing start
- 2016-10-06
- Marketing end
- 2021-08-31
- Substance
- INDAPAMIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 43975-217-10 | 43975021710 | 100 TABLET in 1 BOTTLE (43975-217-10) | 100 tablet | 2016-10-06 | 2021-08-31 | No | No | Current |