CLONIDINE HYDROCHLORIDE
- Product NDC
- 50436-3526
- 11-digit product format
- 504363526
- Labeler code
- 50436
- Product ID
- 50436-3526_47753bc4-dd46-469f-8637-3e5d00641a34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA070923
- Marketing category
- ANDA
- Marketing start
- 1987-09-04
- 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
- 2020-12-31
- 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 |
|---|
| 50436-3526-1 | CLONIDINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET | 30 | | 8 |
| 50436-3526-3 | CLONIDINE HYDROCHLORIDE | 90 in 1 BOTTLE | TABLET | 90 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-3526 | CLONIDINE HYDROCHLORIDE TABLET [UNIT DOSE SERVICES] | 8 | Legacy NDC, 2 package rows | 20190530_8c7e0bca-4855-4018-8bf5-3f9ec5b2e64e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-3526-1 | 50436352601 | 30 in 1 BOTTLE | Historical |
| 50436-3526-3 | 50436352603 | 90 in 1 BOTTLE | Historical |