Prescription drug · ANDA
Desmopressin Acetate NDC 24208-342
Desmopressin acetate .1 mg/mL · Solution · Nasal · Bauch & Lomb Incorporated
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 24208-342-05 | 24208034205 | 1 BOTTLE, PUMP in 1 CARTON (24208-342-05) / 5 mL in 1 BOTTLE, PUMPMarketed from Jan 25, 1999 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Desmopressin Acetate
- Generic name (nonproprietary)
- desmopressin acetate
- Active ingredients
- Desmopressin acetate — .1 mg/mL
- Dosage form
- Solution
- Route
- Nasal
- Labeler
- Bauch & Lomb IncorporatedNDC labeler code 24208
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 074830
- Marketing start
- Marketing end
- Other FDA classes
- Increased Coagulation Factor VIII Activity (Physiologic effect)Increased Coagulation Factor VIII Concentration (Physiologic effect)Vasopressins (Chemical structure)
- Identifiers
- Product ID 24208-342_e7b2ac30-0ad4-4ded-bbc6-c2d50c82917cSPL ID e7b2ac30-0ad4-4ded-bbc6-c2d50c82917cSPL set ID 8ca799f1-7029-4527-9ab4-7512504bb8e2RxCUI 849506UNII XB13HYU18U
- Pharmacologic class
- Factor VIII Activator; Vasopressin Analog
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N424208034205followed by a unit qualifier and the quantityPackage 24208-0342-05. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Desmopressin nasal spray solution is indicated as antidiuretic replacement therapy in the management of central diabetes insipidus in adults and pediatric patients 4 years of age and older. Limitations of Use: Desmopressin nasal spray solution is not indicated for: • Treatment of nephrogenic diabetes insipidus, • Treatment of primary nocturnal enuresis [ see Warnings and Precautions (5.1) ], • Use in patients with conditions that compromise the intranasal route of administration (e.g., severe nasal congestion and blockage, nasal mucosa atrophy, severe atrophic rhinitis, recent nasal surgery such as transsphenoidal hypophysectomy) [see Warnings and Precautions (5.2) ], • Use in patients with …
Excerpt only. Read the full label for complete information.
About NDC 24208-342
- What is NDC 24208-342?
- 24208-342 is the product NDC for Desmopressin Acetate, Desmopressin acetate .1 mg/mL solution, listed with the FDA by Bauch & Lomb Incorporated. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Desmopressin Acetate.
- What is the active ingredient?
- Desmopressin acetate.
- Who is the labeler?
- Bauch & Lomb Incorporated, NDC labeler code 24208. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Desmopressin Acetate?
- 48 other product NDCs are listed under this name. See all Desmopressin Acetate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Desmopressin Acetate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Desmopressin Acetate | Desmopressin acetate 4 ug/mL | Injection, SolutionIntravenous, Subcutaneous | The J. Molner Company LLC | 83148-126 | 83148-0126-01 |
| Desmopressin Acetate | Desmopressin acetate 4 ug/mL | Injection, SolutionIntravenous, Subcutaneous | Armas Pharmaceuticals Inc. | 72485-523 | 72485-0523-10 |
| Desmopressin Acetate | Desmopressin acetate 40 ug/10mL | Injection, SolutionIntravenous, Subcutaneous | Armas Pharmaceuticals Inc. | 72485-524 | 72485-0524-01 |
| Desmopressin Acetate | Desmopressin acetate .1 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4612 | 70518-4612-00 |
| Desmopressin Acetate | Desmopressin acetate 4 ug/mL | Injection, SolutionIntravenous | Caplin Steriles Limited | 65145-183 | 65145-0183-10 |
| Desmopressin Acetate | Desmopressin acetate 4 ug/mL | Injection, SolutionIntravenous | Caplin Steriles Limited | 65145-184 | 65145-0184-01 |
| Desmopressin acetate | Desmopressin acetate 4 ug/mL | InjectionIntravenous, Subcutaneous | Meitheal Pharmaceuticals Inc. | 71288-440 | 71288-0440-02 |
| Desmopressin acetate | Desmopressin acetate 4 ug/mL | InjectionIntravenous, Subcutaneous | Meitheal Pharmaceuticals Inc. | 71288-441 | 71288-0441-10 |
| Desmopressin Acetate | Desmopressin acetate .1 mg/mL | SolutionNasal | Oceanside Pharmaceuticals | 68682-342 | 68682-0342-05 |
| Desmopressin Acetate | Desmopressin acetate 4 ug/mL | Injection, SolutionIntravenous, Subcutaneous | XGen Pharmaceuticals DJB, Inc. | 39822-6200 | 39822-6200-02 |
Other NDCs under ANDA 074830
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Desmopressin Acetate | Desmopressin acetate .1 mg/mL | SolutionNasal | Oceanside Pharmaceuticals | 68682-342 |