Prescription drug · ANDA
Diazepam NDC 80425-0511
Diazepam 10 mg/1 · Tablet · Oral · Advanced Rx of Tennessee, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 80425-0511-1 | 80425051101 | 30 TABLET in 1 BOTTLE (80425-0511-1)Marketed from Apr 14, 2025 | |
| 80425-0511-2 | 80425051102 | 60 TABLET in 1 BOTTLE (80425-0511-2)Marketed from Apr 14, 2025 | |
| 80425-0511-3 | 80425051103 | 90 TABLET in 1 BOTTLE (80425-0511-3)Marketed from Apr 14, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Diazepam
- Generic name (nonproprietary)
- diazepam
- Active ingredients
- Diazepam — 10 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 217843
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Other FDA classes
- Benzodiazepines (Chemical structure)
- Identifiers
- Product ID 80425-0511_32c39455-1398-b87a-e063-6394a90a9597SPL ID 32c39455-1398-b87a-e063-6394a90a9597SPL set ID 32c3af91-a57a-1278-e063-6294a90ae5ecRxCUI 197589UNII Q3JTX2Q7TU
- Pharmacologic class
- Benzodiazepine
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N480425051101followed by a unit qualifier and the quantityPackage 80425-0511-01. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
INDICATIONS AND USAGE Diazepam tablets are indicated for the management of anxiety disorders or for the short- term relief of the symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. In acute alcohol withdrawal, diazepam tablets may be useful in the symptomatic relief of acute agitation, tremor, impending or acute delirium tremens and hallucinosis. Diazepam tablets are a useful adjunct for the relief of skeletal muscle spasm due to reflex spasm to local pathology (such as inflammation of the muscles or joints, or secondary to trauma), spasticity caused by upper motor neuron disorders (such as cerebral palsy…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 217843
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 |
|---|---|---|---|---|
| Diazepam | Diazepam 5 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-653 |
| Diazepam | Diazepam 2 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-652 |
| Diazepam | Diazepam 10 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-654 |
| Diazepam | Diazepam 2 mg/1 | TabletOral | ASCLEMED USA INC. | 76420-314 |
| Diazepam | Diazepam 5 mg/1 | TabletOral | ASCLEMED USA INC. | 76420-315 |
| Diazepam | Diazepam 10 mg/1 | TabletOral | ASCLEMED USA INC. | 76420-316 |
| Diazepam | Diazepam 10 mg/1 | TabletOral | Proficient Rx LP | 82804-186 |
| Diazepam | Diazepam 5 mg/1 | TabletOral | NuCare Pharmaceuticals, Inc. | 68071-3682 |
| Diazepam | Diazepam 5 mg/1 | TabletOral | NuCare Pharmaceuticals, Inc | 68071-3686 |