Clonidine Hydrochloride
- Product NDC
- 72162-2610
- 11-digit product format
- 721622610
- Labeler code
- 72162
- Product ID
- 72162-2610_7fc0f502-5f0d-4085-a84b-a32f6df5583f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA070886
- Marketing category
- ANDA
- Marketing start
- 2021-06-02
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- .2 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Clonidine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CLONIDINE HYDROCHLORIDE | .2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W76I6XXF06 |
| Rxcui | 884185 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2610-5 | Clonidine Hydrochloride | 500 in 1 BOTTLE | TABLET | 500 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2610-5 | 72162261005 | 500 TABLET in 1 BOTTLE (72162-2610-5) | 500 tablet | 2026-04-20 | No | No | Historical |