DILUENT
- Product NDC
- 0781-6021
- 11-digit product format
- 007816021
- Labeler code
- 0781
- Product ID
- 0781-6021_fe80d00e-9eba-4192-9515-f9a5ad686a53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- water solution
- Dosage form
- INJECTION
- Route
- INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Sandoz Inc
- Application
- ANDA203649
- Marketing category
- ANDA
- Marketing start
- 2019-03-25
- Substance
- WATER
- 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
- DILUENT
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WATER | 1 mL/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RUM6K67ESG, 059QF0KO0R |
| Rxcui | 349407, 349408, 349409, 349410 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0781-6021-94 | DILUENT | 1 in 1 CARTON | INJECTION | 1 | | 25 |
| 0781-6021-94 | DILUENT | 50 mL in 1 VIAL | INJECTION | 50 | | 25 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0781-6021 | TREPROSTINIL INJECTION DILUENT (WATER SOLUTION) INJECTION [SANDOZ INC] | 25 | Current NDC, Legacy NDC, 2 package rows | 20230913_473297ca-a872-4052-a053-87dc8f0d3c13.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-6021-94 | 00781602194 | 1 VIAL in 1 CARTON (0781-6021-94) / 50 mL in 1 VIAL | 1 vial | 2019-03-25 | 0000-00-00 | No | No | Current |