Clonidine Hydrochloride
- Product NDC
- 70518-4379
- 11-digit product format
- 705184379
- Labeler code
- 70518
- Product ID
- 70518-4379_38f1df00-4f89-0e69-e063-6394a90a52ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202297
- Marketing category
- ANDA
- Marketing start
- 2025-07-01
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- .3 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Clonidine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CLONIDINE HYDROCHLORIDE | .3 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W76I6XXF06 |
| Rxcui | 884189 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4379-0 | Clonidine Hydrochloride | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4379-0 | 70518437900 | 60 TABLET in 1 BOTTLE, PLASTIC (70518-4379-0) | 60 tablet | 2025-07-01 | No | No | Historical |