clonidine hydrochloride
- Product NDC
- 67296-1196
- 11-digit product format
- 672961196
- Labeler code
- 67296
- Product ID
- 67296-1196_d610062d-3993-dec3-e053-2995a90a9ca1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA078895
- Marketing category
- ANDA
- Marketing start
- 2009-09-21
- 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 |
|---|
| 67296-1196-6 | clonidine hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1196 | CLONIDINE HYDROCHLORIDE TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20220121_4ecb7bdc-4a46-7444-e054-00144ff88e88.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 |
|---|
| 67296-1196-6 | 67296119606 | 60 TABLET in 1 BOTTLE (67296-1196-6) | 60 tablet | 2009-09-21 | 0000-00-00 | No | No | Current |