Dehydrated Alcohol
- Product NDC
- 50090-7643
- 11-digit product format
- 500907643
- Labeler code
- 50090
- Product ID
- 50090-7643_3d1f5a98-a243-4cb4-b59d-6059ba0af173
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- INJECTION, SOLUTION
- Route
- PERCUTANEOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA219400
- Marketing category
- ANDA
- Marketing start
- 2025-06-24
- Substance
- ALCOHOL
- Active strength
- 1 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dehydrated Alcohol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 1 mL/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 2048982 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7643-0 | Dehydrated Alcohol | 5 mL in 1 AMPULE | INJECTION, SOLUTION | 5 | | 1 |
| 50090-7643-0 | Dehydrated Alcohol | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 1 |
| 50090-7643-1 | Dehydrated Alcohol | 2 in 1 CARTON | INJECTION, SOLUTION | 2 | | 1 |
| 50090-7643-1 | Dehydrated Alcohol | 5 mL in 1 AMPULE | INJECTION, SOLUTION | 5 | | 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 |
|---|
| 50090-7643-0 | 50090764300 | 1 AMPULE in 1 CARTON (50090-7643-0) / 5 mL in 1 AMPULE | 1 ampule | 2025-08-27 | No | No | Current |
| 50090-7643-1 | 50090764301 | 2 AMPULE in 1 CARTON (50090-7643-1) / 5 mL in 1 AMPULE | 2 ampule | 2025-08-27 | No | No | Current |