Clorazepate Dipotassium
- Product NDC
- 43063-893
- 11-digit product format
- 430630893
- Labeler code
- 43063
- Product ID
- 43063-893_d6925edc-447e-2bc7-e053-2995a90a9314
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clorazepate Dipotassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA075731
- Marketing category
- ANDA
- Marketing start
- 2000-04-27
- Marketing end
- 0000-00-00
- Substance
- CLORAZEPATE DIPOTASSIUM
- Active strength
- 15 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 Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-893 | CLORAZEPATE DIPOTASSIUM TABLET [PD-RX PHARMACEUTICALS, INC.] | 13 | Legacy NDC | 20250112_6442448e-aa40-40c9-a117-2e689aa5321c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-893-06 | 43063089306 | 6 TABLET in 1 BOTTLE, PLASTIC (43063-893-06) | 6 tablet | 2018-09-12 | 0000-00-00 | No | No | Current |