Prescription drug · ANDA
Alprazolam NDC 71335-0920
Alprazolam 2 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-0920-1 | 7133509200171335092001 | 30 TABLET in 1 BOTTLE (71335-0920-1)Marketed from Aug 2, 2018 | |
| 71335-0920-2 | 7133509200271335092002 | 60 TABLET in 1 BOTTLE (71335-0920-2)Marketed from Dec 28, 2021 | |
| 71335-0920-3 | 7133509200371335092003 | 90 TABLET in 1 BOTTLE (71335-0920-3)Marketed from Dec 28, 2021 | |
| 71335-0920-4 | 7133509200471335092004 | 100 TABLET in 1 BOTTLE (71335-0920-4)Marketed from Dec 28, 2021 | |
| 71335-0920-5 | 7133509200571335092005 | 10 TABLET in 1 BOTTLE (71335-0920-5)Marketed from Dec 28, 2021 | |
| 71335-0920-6 | 7133509200671335092006 | 120 TABLET in 1 BOTTLE (71335-0920-6)Marketed from Dec 28, 2021 | |
| 71335-0920-7 | 7133509200771335092007 | 40 TABLET in 1 BOTTLE (71335-0920-7)Marketed from Dec 28, 2021 |
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)
- Alprazolam
- Generic name (nonproprietary)
- alprazolam
- Active ingredients
- Alprazolam — 2 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 074909
- Marketing start
- Marketing end
- DEA schedule
- CIV
- Other FDA classes
- Benzodiazepines (Chemical structure)
- Identifiers
- Product ID 71335-0920_acde6be9-207c-4954-b94d-7c7777a9188eSPL ID acde6be9-207c-4954-b94d-7c7777a9188eSPL set ID b0000772-2514-45a2-a75d-1bbb13c29989RxCUI 197322UNII YU55MQ3IZY
- 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
N471335092001followed by a unit qualifier and the quantityPackage 71335-0920-01. 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)
Alprazolam tablets are indicated for the: • acute treatment of generalized anxiety disorder (GAD) in adults. • treatment of panic disorder (PD), with or without agoraphobia in adults. Alprazolam tablets are a benzodiazepine indicated for the: • Acute treatment of generalized anxiety disorder in adults. ( 1 ) • Treatment of panic disorder with or without agoraphobia in adults. ( 1 )
Excerpt only. Read the full label for complete information.
About NDC 71335-0920
- What is NDC 71335-0920?
- 71335-0920 is the product NDC for Alprazolam, Alprazolam 2 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Alprazolam.
- What is the active ingredient?
- Alprazolam.
- Who is the labeler?
- Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Alprazolam?
- 124 other product NDCs are listed under this name. See all Alprazolam NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Alprazolam products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Alprazolam | Alprazolam .25 mg/1 | TabletOral | Unichem Pharmaceuticals (USA), Inc. | 29300-360 | 29300-0360-0129300-0360-0529300-0360-10 |
| Alprazolam | Alprazolam .5 mg/1 | TabletOral | Unichem Pharmaceuticals (USA), Inc. | 29300-361 | 29300-0361-0129300-0361-0529300-0361-10 |
| Alprazolam | Alprazolam 1 mg/1 | TabletOral | Unichem Pharmaceuticals (USA), Inc. | 29300-362 | 29300-0362-0129300-0362-0529300-0362-10 |
| Alprazolam | Alprazolam 2 mg/1 | TabletOral | Unichem Pharmaceuticals (USA), Inc. | 29300-363 | 29300-0363-0129300-0363-0529300-0363-10 |
| Alprazolam | Alprazolam 1 mg/1 | TabletOral | Coupler LLC | 67046-0007 | 67046-0007-03 |
| Alprazolam | Alprazolam .5 mg/1 | TabletOral | Coupler LLC | 67046-0154 | 67046-0154-03 |
| Alprazolam | Alprazolam .25 mg/1 | TabletOral | AvPAK | 50268-033 | 50268-0033-15 |
| Alprazolam | Alprazolam .5 mg/1 | TabletOral | AvPAK | 50268-034 | 50268-0034-15 |
| Alprazolam | Alprazolam 1 mg/1 | TabletOral | AvPAK | 50268-035 | 50268-0035-15 |
| Alprazolam | Alprazolam 1 mg/1 | TabletOral | Advanced Rx of Tennessee, LLC | 80425-0444 | 80425-0444-0180425-0444-02 |
Other NDCs under ANDA 074909
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 |
|---|---|---|---|---|
| Alprazolam | Alprazolam 2 mg/1 | TabletOral | Sandoz Inc | 0781-1089 |
| Alprazolam | Alprazolam 2 mg/1 | TabletOral | A-S Medication Solutions | 50090-2819 |
| Alprazolam | Alprazolam 2 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 55289-523 |
| Alprazolam | Alprazolam 2 mg/1 | TabletOral | Proficient Rx LP | 63187-444 |