Clonidine Hydrochloride
- Product NDC
- 67296-0685
- 11-digit product format
- 672960685
- Labeler code
- 67296
- Product ID
- 67296-0685_d5fc32a1-d43e-719a-e053-2a95a90a462b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 2018-01-01
- 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 |
|---|
| 67296-0685-1 | Clonidine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 67296-0685-2 | 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 |
|---|
| 67296-0685 | CLONIDINE HYDROCHLORIDE TABLET [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 2 package rows | 20220120_785f0671-13ba-05f6-e053-2a91aa0a0ec4.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 |
|---|
| 67296-0685-1 | 67296068501 | 30 TABLET in 1 BOTTLE (67296-0685-1) | 30 tablet | 2018-01-01 | 0000-00-00 | No | No | Current |
| 67296-0685-2 | 67296068502 | 60 TABLET in 1 BOTTLE (67296-0685-2) | 60 tablet | 2018-01-01 | 0000-00-00 | No | No | Current |