Diazepam
- Product NDC
- 49999-018
- 11-digit product format
- 499990018
- Labeler code
- 49999
- Product ID
- 49999-018_8eb75d8e-56b5-44af-ad72-ed3ecf72e765
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diazepam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA071321
- Marketing category
- ANDA
- Marketing start
- 2011-11-29
- Marketing end
- 0000-00-00
- Substance
- DIAZEPAM
- Active strength
- 5 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC], Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49999-018 | DIAZEPAM TABLET [QUALITY CARE PRODUCTS LLC] | 3295 | Legacy NDC | 20241218_b5488932-2f9f-4110-af27-82e422d63ed4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49999-018-10 | 49999001810 | 10 TABLET in 1 BOTTLE (49999-018-10) | 10 tablet | 2011-11-29 | 0000-00-00 | No | No | Current |
| 49999-018-20 | 49999001820 | 20 TABLET in 1 BOTTLE (49999-018-20) | 20 tablet | 2011-11-29 | 0000-00-00 | No | No | Current |
| 49999-018-30 | 49999001830 | 30 TABLET in 1 BOTTLE (49999-018-30) | 30 tablet | 2011-11-29 | 0000-00-00 | No | No | Current |
| 49999-018-60 | 49999001860 | 60 TABLET in 1 BOTTLE (49999-018-60) | 60 tablet | 2011-11-29 | 0000-00-00 | No | No | Current |
| 49999-018-90 | 49999001890 | 90 TABLET in 1 BOTTLE (49999-018-90) | 90 tablet | 2011-11-29 | 0000-00-00 | No | No | Current |