Indapamide
- Product NDC
- 50090-7828
- 11-digit product format
- 500907828
- Labeler code
- 50090
- Product ID
- 50090-7828_854e4f89-0eb7-45a9-a302-7d6c08927afd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Indapamide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074299
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Substance
- INDAPAMIDE
- Active strength
- 1.25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Indapamide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| INDAPAMIDE | 1.25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F089I0511L |
| Rxcui | 197815 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7828-0 | Indapamide | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7828-0 | 50090782800 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7828-0) | 2025-12-16 | No | No | Current |