CLONIDINE HYDROCHLORIDE
- Product NDC
- 61919-267
- 11-digit product format
- 619190267
- Labeler code
- 61919
- Product ID
- 61919-267_e9ae16b2-9843-c037-e053-2995a90ab64c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CLONIDINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA078895
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 61919-267-30 | CLONIDINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 61919-267-60 | CLONIDINE HYDROCHLORIDE | 60 in 1 BOTTLE | TABLET | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-267 | CLONIDINE HYDROCHLORIDE TABLET [DIRECTRX] | 4 | Legacy NDC, 2 package rows | 20230418_26dc28bb-2a2e-62d6-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-267-30 | 61919026730 | 30 TABLET in 1 BOTTLE (61919-267-30) | 30 tablet | 2015-01-01 | 0000-00-00 | No | No | Current |
| 61919-267-60 | 61919026760 | 60 TABLET in 1 BOTTLE (61919-267-60) | 60 tablet | 2015-01-01 | 0000-00-00 | No | No | Current |