Desmopressin Acetate
- Product NDC
- 71335-2342
- 11-digit product format
- 713352342
- Labeler code
- 71335
- Product ID
- 71335-2342_c694f562-d5ea-468f-bccf-917437c5d606
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desmopressin Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA019955
- Marketing category
- NDA
- Marketing start
- 2015-12-10
- Substance
- DESMOPRESSIN ACETATE
- Active strength
- .2 mg/1
- Pharmacologic classes
- Factor VIII Activator [EPC], Increased Coagulation Factor VIII Activity [PE], Increased Coagulation Factor VIII Concentration [PE], Vasopressin Analog [EPC], Vasopressins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data
- Finished product
- Yes
- Brand name base
- Desmopressin Acetate
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| DESMOPRESSIN ACETATE | .2 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | XB13HYU18U |
| Rxcui | 833008 |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| XB13HYU18U | DESMOPRESSIN ACETATE | 62357-86-2 | DESMOPRESSIN ACETATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2342-1 | 71335234201 | 90 TABLET in 1 BOTTLE (71335-2342-1) | 90 tablet | 2024-02-06 | No | No | Current |