Diazepam
- Product NDC
- 58118-3927
- 11-digit product format
- 581183927
- Labeler code
- 58118
- Product ID
- 58118-3927_9092bde9-94bc-361f-e053-2995a90aea1b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA071322
- Marketing category
- ANDA
- Marketing start
- 2019-08-20
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 10 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 58118-3927-8 | Diazepam | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58118-3927 | DIAZEPAM TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC] | 1 | Legacy NDC, 1 package rows | 20190821_82359553-4190-4fa7-ae45-18f6e33770d5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 58118-3927-8 | 58118392708 | 30 in 1 BLISTER PACK | Historical |