Desmopressin Acetate
- Product NDC
- 68084-606
- 11-digit product format
- 680840606
- Labeler code
- 68084
- Product ID
- 68084-606_e0e126e7-62ca-77a1-e053-2a95a90a54de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desmopressin Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA076470
- Marketing category
- ANDA
- Marketing start
- 2012-11-06
- 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 |
|---|
| 68084-606-21 | 68084060621 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-606-21) > 1 TABLET in 1 BLISTER PACK (68084-606-11) | 30 blister pack | 2012-11-06 | 0000-00-00 | No | No | Current |