clonidine hydrochloride
- Product NDC
- 63629-7652
- 11-digit product format
- 636297652
- Labeler code
- 63629
- Product ID
- 63629-7652_62f926a8-3359-47f2-afcc-b866e4343793
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 63629-7652-1 | clonidine hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-7652 | CLONIDINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 2 | Legacy NDC, 1 package rows | 20220118_62f926a8-3359-47f2-afcc-b866e4343793.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 |
|---|
| 63629-7652-1 | 63629765201 | 100 TABLET in 1 BOTTLE (63629-7652-1) | 100 tablet | 2019-02-11 | 0000-00-00 | No | No | Current |