Desmopressin Acetate
- Product NDC
- 68151-1281
- 11-digit product format
- 681511281
- Labeler code
- 68151
- Product ID
- 68151-1281_d708db44-7982-4bf1-add5-c854a5cfc71b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desmopressin Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA077122
- Marketing category
- ANDA
- Marketing start
- 2006-01-27
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| bde14c5d-9a3e-43bd-a8e6-0fb00287bdac | Product name | 6 | 20250127 |
| 64db728f-18f9-4c58-ba09-60fd6f75f709 | Product name | 2 | 20190613 |
| aa3ade84-795a-4f84-bfdf-ebe397f656f5 | Product name | 1 | 20190402 |
| d8c9f9fc-e302-45b4-9b21-a802f2592402 | Product name | 1 | 20180810 |
| 4bbcef53-5c79-462a-b7ba-cff48fe1fb5a | Product name | 1 | 20171129 |
| 74cda04a-3bd1-4535-800b-d9b9265e3211 | Product name | 2 | 20171129 |
| 50d55b09-49b8-f134-6bdc-eb6402b911dc | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68151-1281-0 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-0f09-f424-e053-dadaa90a57ce | DESMOPRESSIN ACETATE TABLETS, 0.1 mg and 0.2 mg 7316 7317 Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68151-1281-0 | Desmopressin Acetate | 1 in 1 PACKAGE | TABLET | 1 | 4 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| DESMOPRESSIN ACETATE | ACTIVE INGREDIENT | XB13HYU18U | DESMOPRESSIN ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| DESMOPRESSIN | ACTIVE MOIETY | ENR1LLB0FP | DESMOPRESSIN ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | DESMOPRESSIN ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | DESMOPRESSIN ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | DESMOPRESSIN ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | DESMOPRESSIN ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | DESMOPRESSIN ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68151-1281 | DESMOPRESSIN ACETATE TABLET [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20170724_7954af2c-9c93-4e6d-8814-494aa7b965ad.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 849515 | desmopressin acetate 0.1 MG Oral Tablet | PSN | 7954af2c-9c93-4e6d-8814-494aa7b965ad | 4 |
| 849515 | desmopressin acetate 0.1 MG Oral Tablet | SCD | 7954af2c-9c93-4e6d-8814-494aa7b965ad | 4 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 68151-1281-0 | 68151128100 | 1 in 1 PACKAGE | Historical |