Clonidine Hydrochloride
- Product NDC
- 66116-359
- 11-digit product format
- 661160359
- Labeler code
- 66116
- Product ID
- 66116-359_2c04fc9b-5f83-4a3a-87e3-2b07affd0ad0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MedVantx, Inc.
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 1995-01-03
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 66116-359-30 | Clonidine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66116-359 | CLONIDINE HYDROCHLORIDE TABLET [MEDVANTX, INC.] | 1 | Legacy NDC, 1 package rows | 20111220_2c04fc9b-5f83-4a3a-87e3-2b07affd0ad0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66116-359-30 | 66116035930 | 30 in 1 BOTTLE | Historical |