clonidine hydrochloride
- Product NDC
- 70518-1060
- 11-digit product format
- 705181060
- Labeler code
- 70518
- Product ID
- 70518-1060_5072efc1-e133-4704-e063-6294a90a4277
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091368
- Marketing category
- ANDA
- Marketing start
- 2018-03-13
- 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 |
|---|
| 70518-1060-0 | clonidine hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 5 |
| 70518-1060-1 | clonidine hydrochloride | 50 in 1 BOX | TABLET | 50 | | 5 |
| 70518-1060-2 | clonidine hydrochloride | 1 in 1 POUCH | TABLET | 1 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-1060-0 | 70518106000 | 30 in 1 BLISTER PACK | | | | | Historical |
| 70518-1060-1 | 70518106001 | 50 POUCH in 1 BOX (70518-1060-1) / 1 TABLET in 1 POUCH (70518-1060-2) | 50 pouch | 2026-04-27 | No | No | Current |
| 70518-1060-2 | 70518106002 | 1 in 1 POUCH | | | | | Historical |