Alprazolam
- Product NDC
- 69452-111
- 11-digit product format
- 694520111
- Labeler code
- 69452
- Product ID
- 69452-111_c8370c52-608f-492a-96b1-cc22a5f44035
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bionpharma Inc.
- Application
- ANDA200739
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- Marketing end
- 2019-03-31
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 2ffbe5ef-58ff-88b9-e291-045e0f861f4f | Product name | 4 | 20180827 |
| 1f9e6d58-49d3-d9c1-e570-4bb0466a2c0b | Product name | 1 | 20140508 |
| a1a11520-f3e2-68fa-8bd9-e80b271ef797 | Product name | 1 | 20140508 |
| d153678e-a3c8-bad8-cfe0-385656dde0e7 | Product name | 1 | 20140508 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69452-111-20 | EA - Each | 69452-111 | 11e47979-87d1-435c-adc5-7ad2ab75171d | 1 | 2015-12-02 |
| 69452-111-30 | EA - Each | 69452-111 | 5caabad7-f1d8-4164-85e3-159423c68ac7 | 1 | 2015-12-02 |
| 69452-111-32 | EA - Each | 69452-111 | 09938dd2-af70-4bf4-9f16-eae28766dec0 | 1 | 2015-12-02 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308048 | ALPRAZolam 0.5 MG Oral Tablet | PSN | 81e74e77-398a-45db-a8df-a59bee5c97ad | 4 |
| 308048 | alprazolam 0.5 MG Oral Tablet | SCD | 81e74e77-398a-45db-a8df-a59bee5c97ad | 4 |
| 308048 | ALPRAZolam 0.5 MG Oral Tablet | PSN | 504ba5ad-0a50-4f85-e054-00144ff88e88 | 2 |
| 308048 | alprazolam 0.5 MG Oral Tablet | SCD | 504ba5ad-0a50-4f85-e054-00144ff88e88 | 2 |