Clonidine hydrochloride
- Product NDC
- 55700-802
- 11-digit product format
- 557000802
- Labeler code
- 55700
- Product ID
- 55700-802_017bd5ee-fbb7-4f85-97e0-08371797c4bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA209686
- Marketing category
- ANDA
- Marketing start
- 2019-10-11
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-802 | CLONIDINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [QUALITY CARE PRODUCTS, LLC] | 4 | Legacy NDC | 20241220_e2dc196a-ac63-4cd4-9bb3-cb522599313a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-802-90 | 55700080290 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-802-90) | 2019-10-11 | 0000-00-00 | No | No | Current |