Prescription drug · ANDA
Propranolol Hydrochloride NDC 69238-2080
Propranolol hydrochloride 60 mg/1 · Tablet · Oral · Amneal Pharmaceuticals NY LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69238-2080-1 | 69238208001 | 100 TABLET in 1 BOTTLE (69238-2080-1)Marketed from Jun 3, 2021 |
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)
- Propranolol Hydrochloride
- Generic name (nonproprietary)
- propranolol hydrochloride
- Active ingredients
- Propranolol hydrochloride — 60 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Amneal Pharmaceuticals NY LLCNDC labeler code 69238
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 071976
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic beta-Antagonists (Mechanism)
- Identifiers
- Product ID 69238-2080_d79a3826-466d-4ec4-a0e3-512fdf479235SPL ID d79a3826-466d-4ec4-a0e3-512fdf479235SPL set ID 14d0c95d-418f-40a8-bad3-e20c82424960RxCUI 856448, 856457, 856519, 856556, 856578UNII F8A3652H1VUPC 0369238208016, 0369238207712, 0369238208115, 0369238207910, 0369238207811
- Pharmacologic class
- beta-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
N469238208001followed by a unit qualifier and the quantityPackage 69238-2080-01. 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 Hypertension Propranolol hydrochloride tablets are indicated in the management of hypertension. It may be used alone or used in combination with other antihypertensive agents, particularly a thiazide diuretic. Propranolol hydrochloride is not indicated in the management of hypertensive emergencies. Angina Pectoris Due to Coronary Atherosclerosis Propranolol hydrochloride tablets are indicated to decrease angina frequency and increase exercise tolerance in patients with angina pectoris. Atrial Fibrillation Propranolol hydrochloride tablets are indicated to control ventricular rate in patients with atrial fibrillation and a rapid ventricular response. Myocardial Infarctio…
Excerpt only. Read the full label for complete information.
About NDC 69238-2080
- What is NDC 69238-2080?
- 69238-2080 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 60 mg/1 tablet, listed with the FDA by Amneal Pharmaceuticals NY LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Propranolol Hydrochloride.
- What is the active ingredient?
- Propranolol hydrochloride.
- Who is the labeler?
- Amneal Pharmaceuticals NY LLC, NDC labeler code 69238. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Propranolol Hydrochloride?
- 196 other product NDCs are listed under this name. See all Propranolol Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Propranolol 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) |
|---|---|---|---|---|---|
| Propranolol Hydrochloride | Propranolol hydrochloride 40 mg/1 | TabletOral | American Health Packaging | 60687-948 | 60687-0948-01 |
| Propranolol Hydrochloride | Propranolol hydrochloride 120 mg/1 | Capsule, Extended releaseOral | Creekwood Pharmaceuticals LLC | 82619-134 | 82619-0134-0182619-0134-02 |
| Propranolol Hydrochloride | Propranolol hydrochloride 60 mg/1 | Capsule, Extended releaseOral | Creekwood Pharmaceuticals LLC | 82619-132 | 82619-0132-0182619-0132-02 |
| Propranolol Hydrochloride | Propranolol hydrochloride 80 mg/1 | Capsule, Extended releaseOral | Creekwood Pharmaceuticals LLC | 82619-133 | 82619-0133-0182619-0133-02 |
| Propranolol Hydrochloride | Propranolol hydrochloride 160 mg/1 | Capsule, Extended releaseOral | Creekwood Pharmaceuticals LLC | 82619-135 | 82619-0135-0182619-0135-02 |
| Propranolol Hydrochloride | Propranolol hydrochloride 20 mg/5mL | SolutionOral | PAI Holdings, LLC dba PAI Pharma | 0121-0958 | 00121-0958-16 |
| Propranolol Hydrochloride | Propranolol hydrochloride 20 mg/5mL | SolutionOral | PAI Holdings, LLC dba PAI Pharma | 0121-4958 | 00121-4958-40 |
| Propranolol Hydrochloride | Propranolol hydrochloride 10 mg/1 | TabletOral | Cardinal Health 107, LLC | 55154-2584 | 55154-2584-00 |
| Propranolol Hydrochloride | Propranolol hydrochloride 20 mg/1 | TabletOral | American Health Packaging | 60687-937 | 60687-0937-01 |
| Propranolol Hydrochloride | Propranolol hydrochloride 10 mg/1 | TabletOral | Advanced Rx of Tennessee, LLC | 80425-0583 | 80425-0583-0180425-0583-0280425-0583-03 |
Other NDCs under ANDA 071976
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 |
|---|---|---|---|---|
| Propranolol Hydrochloride | Propranolol hydrochloride 60 mg/1 | TabletOral | Coupler LLC | 67046-1582 |
| Propranolol Hydrochloride | Propranolol hydrochloride 80 mg/1 | TabletOral | Amneal Pharmaceuticals NY LLC | 69238-2081 |