Prescription drug · ANDA
Prazosin hydrochloride NDC 70377-066
Prazosin hydrochloride 1 mg/1 · Capsule · Oral · Biocon Pharma Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70377-066-11 | 7037700661170377006611 | 100 CAPSULE in 1 BOTTLE (70377-066-11)Marketed from Jan 9, 2023 |
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)
- Prazosin hydrochloride
- Generic name (nonproprietary)
- prazosin hydrochloride
- Active ingredients
- Prazosin hydrochloride — 1 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Biocon Pharma Inc.NDC labeler code 70377
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 213406
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic alpha-Antagonists (Mechanism)
- Identifiers
- Product ID 70377-066_99deacbe-59a1-4e72-8b23-d0f470e2633dSPL ID 99deacbe-59a1-4e72-8b23-d0f470e2633dSPL set ID 82a84f69-4742-453f-96c8-532fb7df44c6RxCUI 198141, 312593, 312594UNII X0Z7454B90
- Pharmacologic class
- alpha-Adrenergic Blocker
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
N470377006611followed by a unit qualifier and the quantityPackage 70377-0066-11. 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 Prazosin hydrochloride capsules is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes, including this drug. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than one drug to achieve bl…
Excerpt only. Read the full label for complete information.
About NDC 70377-066
- What is NDC 70377-066?
- 70377-066 is the product NDC for Prazosin hydrochloride, Prazosin hydrochloride 1 mg/1 capsule, listed with the FDA by Biocon Pharma Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Prazosin hydrochloride.
- What is the active ingredient?
- Prazosin hydrochloride.
- Who is the labeler?
- Biocon Pharma Inc., NDC labeler code 70377. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Prazosin hydrochloride?
- 104 other product NDCs are listed under this name. See all Prazosin hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Prazosin hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| prazosin hydrochloride | Prazosin hydrochloride 5 mg/1 | CapsuleOral | Coupler LLC | 67046-1050 | 67046-1050-03 |
| prazosin hydrochloride | Prazosin hydrochloride 1 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-4712 | 70518-4712-00 |
| Prazosin Hydrochloride | Prazosin hydrochloride 1 mg/1 | CapsuleOral | Unit Dose Solutions, Inc. | 87441-067 | 87441-0067-01 |
| Prazosin Hydrochloride | Prazosin hydrochloride 2 mg/1 | CapsuleOral | Unit Dose Solutions, Inc. | 87441-068 | 87441-0068-01 |
| Prazosin Hydrochloride | Prazosin hydrochloride 5 mg/1 | CapsuleOral | Coupler LLC | 67046-0781 | 67046-0781-03 |
| Prazosin Hydrochloride | Prazosin hydrochloride 5 mg/1 | CapsuleOral | Coupler LLC | 67046-1678 | 67046-1678-03 |
| Prazosin Hydrochloride | Prazosin hydrochloride 2 mg/1 | CapsuleOral | Coupler LLC | 67046-0504 | 67046-0504-03 |
| Prazosin Hydrochloride | Prazosin hydrochloride 1 mg/1 | CapsuleOral | Coupler LLC | 67046-0680 | 67046-0680-03 |
| Prazosin Hydrochloride | Prazosin hydrochloride 2 mg/1 | CapsuleOral | Safecor Health LLC | 48433-085 | 48433-0085-20 |
| Prazosin Hydrochloride | Prazosin hydrochloride 1 mg/1 | CapsuleOral | Safecor Health LLC | 48433-084 | 48433-0084-20 |
Other NDCs under ANDA 213406
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 |
|---|---|---|---|---|
| Prazosin hydrochloride | Prazosin hydrochloride 2 mg/1 | CapsuleOral | Biocon Pharma Inc. | 70377-067 |
| Prazosin hydrochloride | Prazosin hydrochloride 5 mg/1 | CapsuleOral | Biocon Pharma Inc. | 70377-068 |
| Prazosin hydrochloride | Prazosin hydrochloride 1 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-3928 |
| Prazosin hydrochloride | Prazosin hydrochloride 2 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-4263 |