Desmopressin Acetate
- Product NDC
- 50268-221
- 11-digit product format
- 502680221
- Labeler code
- 50268
- Product ID
- 50268-221_28af0703-78c8-4206-bfc6-b56c5a3d2827
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desmopressin Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA076470
- Marketing category
- ANDA
- Marketing start
- 2013-07-24
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-221-15 | 50268022115 | 50 BLISTER PACK in 1 BOX (50268-221-15) > 1 TABLET in 1 BLISTER PACK (50268-221-11) | 50 blister pack | 2013-07-24 | 0000-00-00 | No | No | Current |