Desmopressin Acetate
- Product NDC
- 63629-3257
- 11-digit product format
- 636293257
- Labeler code
- 63629
- Product ID
- 63629-3257_e6368593-40cc-4323-ac50-2aaa12b7a35d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desmopressin acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077414
- Marketing category
- ANDA
- Marketing start
- 2006-03-07
- 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
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 |
|---|
| 63629-3257-1 | 63629325701 | 90 TABLET in 1 BOTTLE (63629-3257-1) | 90 tablet | 2024-10-10 | No | No | Historical |