NDC 65862-905-01 - Ipratropium bromide
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
- 65862-905
- Requested NDC
- 65862-905-01
- Package NDCs from labels
- 65862-905-25, 65862-905-33, 65862-905-30, 65862-905-60, 65862-905-01, 65862-905-03
- Manufacturer
- Aurobindo Pharma Limited | Eugia Pharma Specialities Limited, Unit-III
- Effective date
- 2023-10-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| WATER - Aurobindo Pharma Limited | Eugia Pharma Specialities Limited, Unit-III | Aurobindo Pharma Limited | Eugia Pharma Specialities Limited, Unit-III | 2023-10-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65862-905-01 | Ipratropium bromide | 2.5 mL in 1 VIAL, SINGLE-DOSE | SOLUTION | 2.5 | 5 | |
| 65862-905-01 | Ipratropium bromide | 1 in 1 POUCH | SOLUTION | 1 | 5 | |
| 65862-905-03 | Ipratropium bromide | 30 in 1 CARTON | SOLUTION | 30 | 5 | |
| 65862-905-25 | Ipratropium bromide | 25 in 1 POUCH | SOLUTION | 25 | 5 | |
| 65862-905-25 | Ipratropium bromide | 1 in 1 CARTON | SOLUTION | 1 | 5 | |
| 65862-905-30 | Ipratropium bromide | 1 in 1 CARTON | SOLUTION | 1 | 5 | |
| 65862-905-33 | Ipratropium bromide | 30 in 1 POUCH | SOLUTION | 30 | 5 | |
| 65862-905-33 | Ipratropium bromide | 2.5 mL in 1 VIAL, SINGLE-DOSE | SOLUTION | 2.5 | 5 | |
| 65862-905-60 | Ipratropium bromide | 2 in 1 CARTON | SOLUTION | 2 | 5 | |
| 65862-905-60 | Ipratropium bromide | 30 in 1 POUCH | SOLUTION | 30 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 65862-905-25 | ML - Milliliter | 65862-905 | 96adcc8d-04ec-4e80-a441-4ed1c4727266 | 1 | 2017-05-04 |
| 65862-905-30 | ML - Milliliter | 65862-905 | 0b31ef44-e5fe-49a4-8431-8eb5ee4c14dc | 1 | 2017-05-04 |
| 65862-905-60 | ML - Milliliter | 65862-905 | b27ad6c4-11d3-40ac-86fb-557ee9d02d20 | 1 | 2017-05-04 |
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 |
|---|---|---|---|---|---|---|
| Sterile Saline Kids Mist SinuCleanse Breathe | SODIUM CHLORIDE | ASCENT CONSUMER PRODUCTS, INC. | e5c5c313-046f-b0a7-e053-2a95a90a2a07 | 2022-08-08 | Warnings | 451W47IQ8X |
| SODIUM CHLORIDE | SODIUM CHLORIDE | Baxter Healthcare Corporation | 123bd10a-90c7-499e-97f6-acf7e0f0fb4e | 2022-07-29 | Warnings, Adverse reactions | 451W47IQ8X |
| Herplex | ANATHERUM MURICATUM, CLEMATIS ERECTA, MEZEREUM, PHYTOLACCA DECANDRA, RANUNCULUS BULBOSUS, RHUS TOX, THUJA OCCIDENTALIS, NATRUM MURIATICUM, SEPIA | Nashco Products LLC | fad9615f-7004-415d-9f69-ee9ff95f0067 | 2022-07-12 | Warnings | 451W47IQ8X |
| BHI Constipation | DIOSCOREA VILLOSA TUBER, SODIUM CHLORIDE, AND STRYCHNOS NUX-VOMICA SEED | MediNatura Inc | 0365b75b-fee4-4c1d-89ab-c692bdd73f75 | 2022-07-07 | Warnings | 451W47IQ8X |
| Natrium Muriaticum 6X | SODIUM CHLORIDE | Seroyal USA | 0ebf18de-12fe-0bc4-e054-00144ff88e88 | 2022-07-07 | Warnings | 451W47IQ8X |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Hikma Pharmaceuticals USA Inc. | 71bdbbb9-8696-416d-bed4-7259929c0161 | 2022-07-01 | Warnings, Adverse reactions | J697UZ2A9J |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Hikma Pharmaceuticals USA Inc. | 05c56190-e346-4674-a4f8-049ce632ce2d | 2022-07-01 | J697UZ2A9J | |
| Erogetone | ARALIA QUINQUEFOLIA, BERBERIS VULGARIS, CAUSTICUM, CONIUM MACULATUM, DAMIANA, GRAPHITES, LACHESIS MUTUS, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SEPIA | Energique, Inc. | 1e872ecd-e7a5-463d-9832-47b7046096db | 2022-06-28 | Warnings | 451W47IQ8X |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | f42ac50f-0ec5-4713-a4c8-99d972d90bed | 2022-06-22 | Warnings, Adverse reactions | 059QF0KO0R |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | e71c6c83-d518-496c-b2ab-efd5987e4783 | 2022-06-09 | Warnings, Adverse reactions | 059QF0KO0R |
| Cardioplegic Solution | POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, AND MAGNESIUM CHLORIDE | Fresenius Kabi, USA, LLC | eb360dc4-88d6-4b28-9b61-bc359e16bd22 | 2022-05-27 | Warnings, Adverse reactions | 451W47IQ8X |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Sun Pharmaceutical Industries, Inc. | 231ae8f2-1ec9-4e0f-90a8-11d7b6222576 | 2022-04-13 | Warnings, Adverse reactions | 836358 J697UZ2A9J |
| Sodium Chloride | SODIUM CHLORIDE | B. Braun Medical Inc. | 24a08a93-df23-474b-873e-c59ec8855f9f | 2022-03-14 | Warnings, Adverse reactions | 451W47IQ8X |
| Wild Horse 777 Moisturizing Nasal | SODIUM CHLORIDE | Wild Horse 777, Inc. | b0b4dadd-11fa-3dbb-e053-2995a90a2097 | 2022-03-14 | Warnings | 451W47IQ8X |
| Sodium Chloride | SODIUM CHLORIDE | B. Braun Medical Inc. | cc14fafd-3dcd-4fc8-bdbd-6f355c375768 | 2022-02-23 | Warnings, Adverse reactions | 451W47IQ8X |
| Sodium Chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | 8b44bfd3-70a4-4b47-bc7b-590f63b8cc75 | 2022-02-15 | Warnings, Adverse reactions | 451W47IQ8X |
| ACNE HP | CARBO ANIMALIS, ACTIVATED CHARCOAL, POTASSIUM DICHROMATE, SODIUM CHLORIDE, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, SULFUR, ZINC | Natural Creations, Inc. | b2368ab6-e233-4473-99fa-86e1fbc2a879 | 2022-02-14 | Warnings | 451W47IQ8X |
| Sodium Chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | f62481fd-fcdb-4be6-ac13-29c590e925c3 | 2022-02-10 | Adverse reactions | 451W47IQ8X |
| Sterile Water | WATER | American Regent, Inc. | 78b35864-4bbc-4759-a5c1-7e4f25e22932 | 2022-01-31 | Boxed warning | 059QF0KO0R |
| Sodium Chloride | SODIUM CHLORIDE | B. Braun Medical Inc. | e44c41ae-c9c8-4dd8-ba6c-cebb585378aa | 2022-01-31 | Warnings, Adverse reactions | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.