Dichlorphenamide
- Product NDC
- 16571-242
- 11-digit product format
- 165710242
- Labeler code
- 16571
- Product ID
- 16571-242_3ef66eca-f35a-46a8-bebe-b286dfbbb376
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dichlorphenamide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- ANDA218783
- Marketing category
- ANDA
- Marketing start
- 2025-11-18
- Substance
- DICHLORPHENAMIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA], Sulfonamides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dichlorphenamide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DICHLORPHENAMIDE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VVJ6673MHY |
| Rxcui | 197594 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16571-242-01 | Dichlorphenamide | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 16571-242-01 | 16571024201 | 100 TABLET in 1 BOTTLE (16571-242-01) | 100 tablet | 2025-11-18 | No | No | Historical |