Alprazolam
- Product NDC
- 66336-932
- 11-digit product format
- 663360932
- Labeler code
- 66336
- Product ID
- 66336-932_dfa9fa44-a29c-4f1f-9249-23ecd9e2efdf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Dispensing Solutions, Inc.
- Application
- ANDA078491
- Marketing category
- ANDA
- Marketing start
- 2008-09-25
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
NDC, Effective, Action table| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|
| 66336-932-10 | 2019-11-13 | C162847 | 48780-1 | 97449f38-b846-f6ea-e053-dbdaa90aa703 | ALPRAZOLAM TABLETS, USP 0.25 mg, 0.5 mg, 1 mg and 2 mg |
| 66336-932-30 | 2019-11-13 | C162847 | 48780-1 | 97449f38-b846-f6ea-e053-dbdaa90aa703 | ALPRAZOLAM TABLETS, USP 0.25 mg, 0.5 mg, 1 mg and 2 mg |
| 66336-932-60 | 2019-11-13 | C162847 | 48780-1 | 97449f38-b846-f6ea-e053-dbdaa90aa703 | ALPRAZOLAM TABLETS, USP 0.25 mg, 0.5 mg, 1 mg and 2 mg |
| 66336-932-90 | 2019-11-13 | C162847 | 48780-1 | 97449f38-b846-f6ea-e053-dbdaa90aa703 | ALPRAZOLAM TABLETS, USP 0.25 mg, 0.5 mg, 1 mg and 2 mg |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66336-932-10 | Alprazolam | 10 in 1 BOTTLE | TABLET | 10 | | 1 |
| 66336-932-30 | Alprazolam | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 66336-932-60 | Alprazolam | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 66336-932-90 | Alprazolam | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| ALPRAZOLAM | ACTIVE INGREDIENT | YU55MQ3IZY | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| ALPRAZOLAM | ACTIVE MOIETY | YU55MQ3IZY | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| DOCUSATE SODIUM | INACTIVE INGREDIENT | F05Q2T2JA0 | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| FD&C BLUE NO. 1 | INACTIVE INGREDIENT | H3R47K3TBD | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66336-932 | ALPRAZOLAM TABLET [DISPENSING SOLUTIONS, INC.] | 1 | Legacy NDC, 4 package rows | 20120215_0d97256b-77f5-405e-b5be-cded19653180.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66336-932-10 | 66336093210 | 10 in 1 BOTTLE | Historical |
| 66336-932-30 | 66336093230 | 30 in 1 BOTTLE | Historical |
| 66336-932-60 | 66336093260 | 60 in 1 BOTTLE | Historical |
| 66336-932-90 | 66336093290 | 90 in 1 BOTTLE | Historical |