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NDC 00703-5051-03 Desmopressin acetate 4 ug/mL Details
Desmopressin acetate 4 ug/mL
Desmopressin acetate is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Teva Parenteral Medicines, Inc.. The primary component is DESMOPRESSIN ACETATE.
Product Information
| NDC | 00703-5051 |
|---|---|
| Product ID | 0703-5051_85956c95-660a-4d31-a78a-3ee4c379f325 |
| Associated GPIs | 30201010102030 |
| GCN Sequence Number | 006616 |
| GCN Sequence Number Description | desmopressin acetate VIAL 4 MCG/ML INJECTION |
| HIC3 | P2B |
| HIC3 Description | ANTIDIURETIC AND VASOPRESSOR HORMONES |
| GCN | 10260 |
| HICL Sequence Number | 002841 |
| HICL Sequence Number Description | DESMOPRESSIN ACETATE |
| Brand/Generic | Generic |
| Proprietary Name | Desmopressin acetate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Desmopressin acetate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 4 |
| Active Ingredient Units | ug/mL |
| Substance Name | DESMOPRESSIN ACETATE |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Pharmaceutical Class | Factor VIII Activator [EPC], Increased Coagulation Factor VIII Activity [PE], Increased Coagulation Factor VIII Concentration [PE], Vasopressin Analog [EPC], Vasopressins [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA074888 |
| Listing Certified Through | 2022-12-31 |
Package
NDC 00703-5051-03 (00703505103)
| NDC Package Code | 0703-5051-03 |
|---|---|
| Billing NDC | 00703505103 |
| Package | 10 VIAL in 1 TRAY (0703-5051-03) / 1 mL in 1 VIAL (0703-5051-01) |
| Marketing Start Date | 1997-11-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |