Desmopressin Acetate
- Product NDC
- 70518-3493
- 11-digit product format
- 705183493
- Labeler code
- 70518
- Product ID
- 70518-3493_e7144621-d26e-2d75-e053-2a95a90adc9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desmopressin Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207880
- Marketing category
- ANDA
- Marketing start
- 2022-08-22
- 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 |
|---|
| 70518-3493-0 | 70518349300 | 100 POUCH in 1 BOX (70518-3493-0) > 1 TABLET in 1 POUCH (70518-3493-1) | 100 pouch | 2022-08-22 | 0000-00-00 | No | No | Current |