NDC 72162-2198-01 - Nadolol
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 72162-2198
- Requested NDC
- 72162-2198-01
- Package NDCs from labels
- 72162-2198-1, 72162-2198-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2026-03-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Nadolol - Bryant Ranch Prepack | Bryant Ranch Prepack | 2026-03-19 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72162-2198-1 | Nadolol | 100 in 1 BOTTLE | TABLET | 100 | 103 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72162-2198 | NADOLOL TABLET [BRYANT RANCH PREPACK] | 102 | Current NDC, 1 package rows | 20241122_2d126308-c58d-4950-9dcb-eaadb1a2054f.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72162-2198-1 | EA - Each | 72162-2198 | c5a87270-04db-409a-871a-49b9f2311498 | 1 | 2024-01-04 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Nadolol | NADOLOL | Bryant Ranch Prepack | 0d66548a-231e-4104-be0c-c6ce1586b46c | 2024-10-02 | Warnings, Adverse reactions | 198008 FEN504330V |
| Sodium Citrate and Citric Acid | SODIUM CITRATE AND CITRIC ACID | Chartwell RX, LLC | 525136c9-7758-437b-b57b-94b905786825 | 2024-05-31 | Adverse reactions | 2968PHW8QP |
| Nadolol | NADOLOL | BluePoint Laboratories | 0a2acdc0-aab6-462e-a377-67a0f3d55ec6 | 2024-05-28 | Boxed warning, Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| Pure Cornstarch Baby | CORN STARCH | Walgreen Company | d0e9bd13-b568-4f7e-b036-8d23e71ad8bf | 2024-03-25 | Warnings | O8232NY3SJ |
| Nadolol | NADOLOL | Bryant Ranch Prepack | 2fc1f850-9653-4082-929a-926b644810e7 | 2024-01-26 | Boxed warning, Warnings, Adverse reactions | 198006 FEN504330V |
| Nadolol | NADOLOL | Bryant Ranch Prepack | 9cf4ca73-2d38-44c2-a522-d44d536b5e55 | 2024-01-26 | Boxed warning, Warnings, Adverse reactions | 198007 FEN504330V |
| Nadolol | NADOLOL | Aurobindo Pharma Limited | 44c5352d-89f8-4bd3-9479-1069304562ca | 2024-01-10 | Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| NADOLOL | NADOLOL | Alembic Pharmaceuticals Inc. | 6ab029aa-dfe0-4abb-8c7f-2692fe6a2368 | 2024-01-08 | Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| Nadolol | NADOLOL | Zydus Pharmaceuticals USA Inc. | a0a38f9b-268d-4463-881d-5bee6cd92e8a | 2024-01-02 | Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| Nadolol | NADOLOL | Exelan Pharmaceuticals Inc. | 5c6737f8-8fd8-4d8f-a66a-e99d3b64e1dd | 2024-01-01 | Boxed warning, Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| Nadolol | NADOLOL | Cipla USA Inc. | c899eedb-4113-45da-acc3-8e181250a7d8 | 2024-01-01 | Boxed warning, Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| Oracit | CITRIC ACID AND SODIUM CITRATE | CMP Pharma, Inc. | bc26abed-8e6e-475d-8ab3-abf7d0377003 | 2023-12-07 | Adverse reactions | 2968PHW8QP |
| Phexxi | LACTIC ACID, L-, CITRIC ACID MONOHYDRATE, AND POTASSIUM BITARTRATE | Evofem, Inc. | 173ff411-7227-47b0-94dc-844e1ebaf14e | 2023-11-21 | Warnings, Adverse reactions | 2968PHW8QP |
| NADOLOL | NADOLOL | VGYAAN Pharmaceuticals LLC | 85b4b931-51c4-4326-88ea-708dde8323d4 | 2023-09-22 | Boxed warning, Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| NADOLOL | NADOLOL | Alembic Pharmaceuticals Limited | 0bd202e3-c673-4945-b828-1a5bc6a896ae | 2023-06-08 | Warnings, Adverse reactions | 198007 198006 198008 FEN504330V |
| GUNA FLAM RELIEF | ACONITUM NAPELLUS - APIS MELLIFERA - ARNICA MONTANA WHOLE - ATROPA BELLADONNA - BASIC CUPRIC CARBONATE - BRYONIA ALBA ROOT - MATRICARIA CHAMOMILLA WHOLE - CALCIUM SULFIDE - CITRIC ACID MONOHYDRATE - ECHINACEA ANGUSTIFOLIA - FERRIC PHOSPHATE - PHYTOLACCA AMERICANA ROOT - RANCID BEEF - SODIUM PYRUVATE - PORK LIVER - RANCID BEEF - SUS SCROFA PITUITARY GLAND - | Guna spa | af5a9c74-e1c7-6574-e053-2995a90a3d10 | 2020-09-15 | Warnings | 2968PHW8QP |
| GUNA-ALLERGY-PREV | AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12 - INTERFERON GAMMA-1B - MANGANESE GLUCONATE - PARIETARIA OFFICINALIS - PHLEUM PRATENSE - SODIUM PYRUVATE - SODIUM SULFATE - SUCCINIC ACID - SULFUR - URTICA URENS - VIBURNUM OPULUS ROOT - WYETHIA HELENIOIDES ROOT - | Guna spa | adae93c0-1de9-4e45-ab58-148171f0dc86 | 2018-12-21 | Warnings | 2968PHW8QP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.