Diazepam
- Product NDC
- 66336-033
- 11-digit product format
- 663360033
- Labeler code
- 66336
- Product ID
- 66336-033_c55cb2d2-2cba-4ca3-b0ef-50c003b920de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Dispensing Solutions, Inc.
- Application
- ANDA077749
- Marketing category
- ANDA
- Marketing start
- 2006-03-31
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 10 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66336-033-94 | Diazepam | 120 in 1 BOTTLE, PLASTIC | TABLET | 120 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66336-033 | DIAZEPAM TABLET [DISPENSING SOLUTIONS, INC.] | 2 | Legacy NDC, 1 package rows | 20131107_c7bcabfd-596d-4204-a560-f75caa250249.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66336-033-94 | 66336003394 | 120 in 1 BOTTLE, PLASTIC | Historical |