Prescription drug · ANDA
Clonidine Hydrochloride NDC 59651-233
Clonidine hydrochloride .2 mg/1 · Tablet · Oral · Aurobindo Pharma Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 59651-233-01 | 59651023301 | 100 TABLET in 1 BOTTLE (59651-233-01)Marketed from Jun 2, 2021 | |
| 59651-233-05 | 59651023305 | 500 TABLET in 1 BOTTLE (59651-233-05)Marketed from Jun 2, 2021 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Clonidine Hydrochloride
- Generic name (nonproprietary)
- clonidine hydrochloride
- Active ingredients
- Clonidine hydrochloride — .2 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Aurobindo Pharma Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 070886
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic alpha2-Agonists (Mechanism)
- Identifiers
- Product ID 59651-233_2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fbSPL ID 2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fbSPL set ID 2b75c20c-9dcc-4a63-854a-e9cdd2d7c1fbRxCUI 884173, 884185, 884189UNII W76I6XXF06
- Pharmacologic class
- Central alpha-2 Adrenergic Agonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N459651023301followed by a unit qualifier and the quantityPackage 59651-0233-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE Clonidine hydrochloride tablets are indicated in the treatment of hypertension. Clonidine hydrochloride tablets may be employed alone or concomitantly with other antihypertensive agents.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 070886
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Clonidine Hydrochloride | Clonidine hydrochloride .1 mg/1 | TabletOral | A-S Medication Solutions | 50090-6744 |
| Clonidine Hydrochloride | Clonidine hydrochloride .2 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2610 |
| Clonidine Hydrochloride | Clonidine hydrochloride .1 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2609 |
| Clonidine Hydrochloride | Clonidine hydrochloride .3 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2611 |
| Clonidine Hydrochloride | Clonidine hydrochloride .1 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-232 |
| Clonidine Hydrochloride | Clonidine hydrochloride .3 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-234 |