NDC 70954-159-40 - Clorazepate Dipotassium
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
- 70954-159
- Requested NDC
- 70954-159-40
- Package NDCs from labels
- 70954-159-10, 70954-159-20, 70954-159-30, 70954-159-40, 70954-159-50
- Manufacturer
- ANI Pharmaceuticals, Inc. | Novitium Pharma LLC
- Effective date
- 2025-08-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Clorazepate Dipotassium - ANI Pharmaceuticals, Inc. | Novitium Pharma LLC | ANI Pharmaceuticals, Inc. | Novitium Pharma LLC | 2025-08-12 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70954-159-10 | Clorazepate Dipotassium | 100 in 1 BOTTLE | TABLET | 100 | 13 | |
| 70954-159-20 | Clorazepate Dipotassium | 500 in 1 BOTTLE | TABLET | 500 | 13 | |
| 70954-159-30 | Clorazepate Dipotassium | 30 in 1 BOTTLE | TABLET | 30 | 13 | |
| 70954-159-40 | Clorazepate Dipotassium | 1 in 1 BLISTER PACK | TABLET | 1 | 13 | |
| 70954-159-50 | Clorazepate Dipotassium | 30 in 1 BOX, UNIT-DOSE | TABLET | 30 | 13 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70954-159-10 | EA - Each | 70954-159 | 4d201f37-b4a8-49b9-a0d4-427f95511aea | 1 | 2022-07-06 |
| 70954-159-30 | EA - Each | 70954-159 | 66ddfa29-e746-4559-a6b5-94c2869fe137 | 1 | 2023-09-05 |
| 70954-159-40 | EA - Each | 70954-159 | ef021671-4401-4255-978d-e5a694e8b1fc | 1 | 2025-07-08 |
| 70954-159-50 | EA - Each | 70954-159 | 195dbf33-cf57-4b67-aabb-f74d7704ab06 | 1 | 2025-07-08 |
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 |
|---|---|---|---|---|---|---|
| Magnesium Oxide | MAGNESIUM OXIDE | Method Pharmaceuticals, LLC | 0af63651-f9d9-43b9-b6f0-4878466a82e6 | 2025-10-21 | Warnings | 3A3U0GI71G |
| Potassium chloride | POTASSIUM CHLORIDE | Macleods Pharmaceuticals Limited | e0562a05-4359-4256-87e3-fcde65a008cd | 2025-10-18 | Warnings, Adverse reactions | 660YQ98I10 |
| Mold Relief Formula | KALI MURIATICUM, GELSEMIUM, KALI BICHROMICUM, SABADILLA, HISTAMINUM, MOLD MIX. | Integrative Healing Institute, LLC | 067ee707-7219-4370-9cdd-08888f45b5e5 | 2025-10-17 | Warnings | 660YQ98I10 |
| Seasonal Allergy Formula | HYDRASTIS CANADENSIS, KALI MURIATICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM, SABADILLA, HISTAMINUM, HOUSE DUST, GRASS MIX, TREES MIX, WEEDS MIX | Integrative Healing Institute, LLC | 1d4deee9-5452-421b-a107-ab150d1f6214 | 2025-10-17 | Warnings | 660YQ98I10 |
| KLOR-CON M | POTASSIUM CHLORIDE | Cardinal Health 107, LLC | ee3a1815-7325-4838-9764-fe1db68877b6 | 2025-10-17 | Warnings, Adverse reactions | 660YQ98I10 |
| DENTI BUONGIORNO PEACH MINT WHITENING TOOTH | HYDROGEN PEROXIDE, SILICA | ATOSAFE CO., Ltd | 41196c2f-8e2e-a54d-e063-6294a90ad8a7 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PEACH MINT WHITENING TOOTH | HYDROGEN PEROXIDE, SILICA | DONG IL PHARMS CO.,LTD | 41198822-7c8f-ceb2-e063-6394a90a4373 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO ORIGINAL TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 41197bb6-f6f4-c86d-e063-6294a90ad476 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO ORIGINAL TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 4114ab09-1115-6b0b-e063-6394a90ab442 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | ATOSAFE CO., Ltd | 41155922-d7ac-0a7a-e063-6294a90afe48 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | DONG IL PHARMS CO.,LTD | 41157552-2473-176b-e063-6294a90a9ad0 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | ATOSAFE CO., Ltd | 4115d122-3090-d3e5-e063-6294a90aafb6 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | DONG IL PHARMS CO.,LTD | 4115b653-63ff-703f-e063-6294a90a652a | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| Silicea Belladonna | SILICEA BELLADONNA | Uriel Pharmacy Inc. | a142eb87-c5fb-4138-bc98-e7f1391fe221 | 2025-10-10 | Warnings | ETJ7Z6XBU4 |
| Potassium Chloride | POTASSIUM CHLORIDE | Strides Pharma Science Limited | f4e36462-3522-4130-8785-6c18871d2984 | 2025-10-10 | Warnings, Adverse reactions | 660YQ98I10 |
| Magnesium Oxide | MAGNESIUM OXIDE | A-S Medication Solutions | c14d2b4d-d6d8-4293-835e-5d893d5b7e6a | 2025-10-10 | Warnings | 3A3U0GI71G |
| Potassium Chloride | POTASSIUM CHLORIDE | Northstar Rx LLC | fbed8c29-b3f1-4e53-b290-6f717290cecf | 2025-10-07 | Warnings, Adverse reactions | 660YQ98I10 |
| Homeopathic Calm Drops | ARSENIC TRIOXIDE 30C, MATRICARIA CHAMOMILLA12X, ARABICA COFFEE BEAN 30X, POTASSIUM CARBONATE30C, STRYCHNOS IGNATII SEED30X, LACHESIS MUTA VENOM12X, PHOSPHORIC ACID 3X, ANEMONE PULSATILLA 12C, VALERIAN 30C, ACONITUM NAPELLUS 6X, CHLORIDE ION 12X, STRYCHNOS NUX-VOMICA SEED 30C | HISTORICAL REMEDIES LLP. | 69c35bc2-b9a0-4bb4-a56d-0e2d1c3f7958 | 2025-10-07 | Warnings | BQN1B9B9HA |
| Parathyropar | SYMPHYTUM OFFICINALE, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HEKLA LAVA, MANGANUM METALLICUM, RHUS TOX, SILICEA, PARATHORMONUM | Energique, Inc. | bd13617a-c470-4421-8f47-43a98036f40b | 2025-10-06 | Warnings | ETJ7Z6XBU4 |
| Mitochondria PRO | ARALIA QUINQUEFOLIA, ARNICA MONTANA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALPHA-KETOGLUTARICUM ACIDUM, ASCORBICUM ACIDUM, ALPHA-LIPOICUM ACIDUM, CALCAREA CARBONICA, CITRICUM ACIDUM, CUPRUM METALLICUM, CYSTEINUM, FERRUM METALLICUM, IODIUM, LEVOTHYROXINUM, MAGNESIUM GLUCONICUM DIHYDRICUM, MALICUM ACIDUM, MANGANUM ACETICUM, NADIDUM, NATRUM PYRUVICUM, NICOTINAMIDUM, PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, SELENIUM METALLICUM, SULPHUR, THIAMINUM HYDROCHLORICUM, UBIDECARENONUM, ZINCUM METALLICUM, | Energique, Inc. | 8c3e961d-bc33-40cd-a282-a4fe5aa3f0ad | 2025-10-06 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.