Desmopressin Acetate
- Product NDC
- 0591-2465
- 11-digit product format
- 005912465
- Labeler code
- 0591
- Product ID
- 0591-2465_f1a3927d-c80e-48cf-9079-9c50406879be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desmopressin Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA076470
- Marketing category
- ANDA
- Marketing start
- 2011-08-15
- Marketing end
- 0000-00-00
- Substance
- DESMOPRESSIN ACETATE
- Active strength
- 0 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0591-2465-01 | 00591246501 | 100 TABLET in 1 BOTTLE, PLASTIC (0591-2465-01) | 100 tablet | 2011-08-15 | 0000-00-00 | No | No | Current |