Prescription drug · ANDA
Amlodipine and Benazepril Hydrochloride NDC 57237-147
Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1 · Capsule · Oral · Rising Pharma Holdings, Inc.
NDC codes
FDA NDC DirectoryProduct NDC (as listed)57237-147Labeler and product segments. Claims need a package NDC.
Product NDC at billing width57237-0147Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 57237-147-01 | 57237014701 | 100 CAPSULE in 1 BOTTLE (57237-147-01)Marketed from Sep 5, 2012 | |
| 57237-147-05 | 57237014705 | 500 CAPSULE in 1 BOTTLE (57237-147-05)Marketed from Sep 5, 2012 |
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)
- Amlodipine and Benazepril Hydrochloride
- Generic name (nonproprietary)
- amlodipine and benazepril hydrochloride
- Active ingredients
- Amlodipine besylate — 10 mg/1Benazepril hydrochloride — 40 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Rising Pharma Holdings, Inc.NDC labeler code 57237
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 202239
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin-converting Enzyme Inhibitors (Mechanism)Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)Dihydropyridines (Chemical structure)
- Identifiers
- Product ID 57237-147_a4aff76f-e9a9-4300-b42c-616d8ca55d5dSPL ID a4aff76f-e9a9-4300-b42c-616d8ca55d5dSPL set ID 03b175fc-d430-490d-b7ac-9f7a2cb1dd8bRxCUI 898342, 898346, 898350, 898353, 898356, 898359UNII 864V2Q084H, N1SN99T69TUPC 0357237143018, 0357237142011, 0357237146019, 0357237147016, 0357237145012, 0357237144015
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel 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
N457237014701followed by a unit qualifier and the quantityPackage 57237-0147-01. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
Amlodipine and benazepril hydrochloride capsules are a combination capsule of amlodipine, a dihydropyridine calcium channel blocker (DHP CCB) and benazepril, an angiotensin-converting enzyme (ACE) inhibitor. Amlodipine and benazepril hydrochloride capsules are indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent. (1) 1.1 Hypertension Amlodipine and benazepril hydrochloride capsules are indicated for the treatment of hypertension in patients not adequately controlled on monotherapy with either agent.
Excerpt only. Read the full label for complete information.
About NDC 57237-147
- What is NDC 57237-147?
- 57237-147 is the product NDC for Amlodipine and Benazepril Hydrochloride, Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1 capsule, listed with the FDA by Rising Pharma Holdings, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Amlodipine and Benazepril Hydrochloride.
- What is the active ingredient?
- Amlodipine besylate, Benazepril hydrochloride.
- Who is the labeler?
- Rising Pharma Holdings, Inc., NDC labeler code 57237. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Amlodipine and Benazepril Hydrochloride?
- 39 other product NDCs are listed under this name. See all Amlodipine and Benazepril Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Amlodipine and Benazepril 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) |
|---|---|---|---|---|---|
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1 | CapsuleOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-923 | 23155-0923-0123155-0923-0523155-0923-10 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-924 | 23155-0924-0123155-0924-0523155-0924-10 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1 | CapsuleOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-921 | 23155-0921-0123155-0921-0523155-0921-10 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-922 | 23155-0922-0123155-0922-0523155-0922-10 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1 | CapsuleOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-920 | 23155-0920-0123155-0920-0523155-0920-10 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1 | CapsuleOral | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 23155-925 | 23155-0925-0123155-0925-0523155-0925-10 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Preferred Pharmaceuticals Inc. | 68788-8454 | 68788-8454-03 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Northwind Health Company, LLC | 51655-213 | 51655-0213-2651655-0213-52 |
| Amlodipine And Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | DIRECT RX | 72189-260 | 72189-0260-90 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-1928 | 70518-1928-00 |
Other NDCs under ANDA 202239
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 |
|---|---|---|---|---|
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-4284 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Aurobindo Pharma Limited | 65862-584 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 2.5 mg/1; Benazepril hydrochloride 10 mg/1 | CapsuleOral | Aurobindo Pharma Limited | 65862-582 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1 | CapsuleOral | Aurobindo Pharma Limited | 65862-583 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1 | CapsuleOral | Aurobindo Pharma Limited | 65862-585 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Aurobindo Pharma Limited | 65862-586 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1 | CapsuleOral | Aurobindo Pharma Limited | 65862-587 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-1928 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 40 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-2720 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Preferred Pharmaceuticals Inc. | 68788-8454 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Bryant Ranch Prepack | 71335-0953 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | PD-Rx Pharmaceuticals, Inc. | 72789-285 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-7361 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 10 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-6770 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 40 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-3357 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Proficient Rx LP | 71205-122 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | Northwind Health Company, LLC | 51655-213 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 5 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-1042 |
| Amlodipine And Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | DIRECT RX | 72189-260 |
| Amlodipine and Benazepril Hydrochloride | Amlodipine besylate 10 mg/1; Benazepril hydrochloride 20 mg/1 | CapsuleOral | PD-Rx Pharmaceuticals, Inc. | 72789-412 |
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