Prescription drug · ANDA
Clonidine hydrochloride NDC 71335-0922
Clonidine hydrochloride .1 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-0922-0 | 71335092200 | 24 TABLET in 1 BOTTLE (71335-0922-0)Marketed from Dec 28, 2021 | |
| 71335-0922-1 | 71335092201 | 100 TABLET in 1 BOTTLE (71335-0922-1)Marketed from Dec 28, 2021 | |
| 71335-0922-2 | 71335092202 | 30 TABLET in 1 BOTTLE (71335-0922-2)Marketed from Aug 28, 2018 | |
| 71335-0922-3 | 71335092203 | 20 TABLET in 1 BOTTLE (71335-0922-3)Marketed from Dec 28, 2021 | |
| 71335-0922-4 | 71335092204 | 60 TABLET in 1 BOTTLE (71335-0922-4)Marketed from Mar 31, 2020 | |
| 71335-0922-5 | 71335092205 | 120 TABLET in 1 BOTTLE (71335-0922-5)Marketed from Mar 3, 2020 | |
| 71335-0922-6 | 71335092206 | 90 TABLET in 1 BOTTLE (71335-0922-6)Marketed from Aug 3, 2018 | |
| 71335-0922-7 | 71335092207 | 10 TABLET in 1 BOTTLE (71335-0922-7)Marketed from Sep 25, 2018 | |
| 71335-0922-8 | 71335092208 | 45 TABLET in 1 BOTTLE (71335-0922-8)Marketed from Dec 28, 2021 | |
| 71335-0922-9 | 71335092209 | 14 TABLET in 1 BOTTLE (71335-0922-9)Marketed from Jan 16, 2020 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — .1 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 070925
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic alpha2-Agonists (Mechanism)
- Identifiers
- Product ID 71335-0922_1a487aeb-d565-4e30-b410-1c007e262560SPL ID 1a487aeb-d565-4e30-b410-1c007e262560SPL set ID cee049ea-a476-433c-971f-2466a6a3263bRxCUI 884173UNII 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
N471335092200followed by a unit qualifier and the quantityPackage 71335-0922-00. 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 USP are indicated in the treatment of hypertension. Clonidine hydrochloride tablets USP may be employed alone or concomitantly with other antihypertensive agents.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 070925
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 | NuCare Pharmaceuticals,Inc. | 68071-4545 |
| Clonidine hydrochloride | Clonidine hydrochloride .1 mg/1 | TabletOral | Asclemed USA, Inc. | 76420-283 |
| Clonidine hydrochloride | Clonidine hydrochloride .1 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-3987 |
| Clonidine hydrochloride | Clonidine hydrochloride .1 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-445 |
| Clonidine hydrochloride | Clonidine hydrochloride .1 mg/1 | TabletOral | Proficient Rx LP | 71205-588 |
| Clonidine Hydrochloride | Clonidine hydrochloride .1 mg/1 | TabletOral | Proficient Rx LP | 63187-202 |