NDC 68084-952-95 - Albuterol Sulfate
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
- 68084-952
- Requested NDC
- 68084-952-95
- Package NDCs from labels
- 68084-952-95, 68084-952-25
- Manufacturer
- American Health Packaging
- Effective date
- 2024-07-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Albuterol Sulfate - American Health Packaging | American Health Packaging | 2024-07-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68084-952-25 | Albuterol Sulfate | 30 in 1 BOX, UNIT-DOSE | TABLET | 30 | 5 | |
| 68084-952-95 | Albuterol Sulfate | 1 in 1 BLISTER PACK | TABLET | 1 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68084-952-25 | EA - Each | 68084-952 | 10932747-c4cb-4e52-981f-44aee28ec466 | 1 | 2015-11-12 |
| 68084-952-95 | EA - Each | 68084-952 | 74e13657-2856-4a7c-a03d-05342393dbb1 | 1 | 2015-11-12 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| albuterol sulfate | ACTIVE INGREDIENT | 021SEF3731 | ALBUTEROL SULFATE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| albuterol | ACTIVE MOIETY | QF8SVZ843E | ALBUTEROL SULFATE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| anhydrous lactose | INACTIVE INGREDIENT | 3SY5LH9PMK | ALBUTEROL SULFATE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | ALBUTEROL SULFATE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| sodium starch glycolate type a potato | INACTIVE INGREDIENT | 5856J3G2A2 | ALBUTEROL SULFATE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| starch, corn | INACTIVE INGREDIENT | O8232NY3SJ | ALBUTEROL SULFATE TABLET [AMERICAN HEALTH PACKAGING] | 1 |
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 |
|---|---|---|---|---|---|---|
| Lotrimin Daily Sweat and Odor Control | TOPICAL STARCH | Bayer HealthCare LLC. | 9ec5c80d-b550-496f-e053-2a95a90a5489 | 2026-01-16 | Warnings | O8232NY3SJ |
| Albuterol Sulfate | ALBUTEROL SULFATE | Preferred Pharmaceuticals Inc. | 5de6a189-a8b7-4b33-b162-add6b6e4b275 | 2026-01-16 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Preferred Pharmaceuticals Inc. | d6acb5a7-555a-463a-ae65-2911d6789b42 | 2026-01-14 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol | ALBUTEROL SULFATE | Cipla USA Inc. | fd0389e0-3713-42e0-8ef2-3bb97676fded | 2026-01-04 | Warnings, Adverse reactions | 021SEF3731 |
| Medicated Cornstarch Baby Powder | ACTIVE CORN STARCH | Davion, Inc. | e39032d1-c8cd-4a41-af10-126970b8ad38 | 2025-12-29 | Warnings | O8232NY3SJ |
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | Chartwell Governmental & Specialty RX, LLC. | dd47559a-84f6-42a5-a00e-48754505418e | 2025-12-17 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Sandoz Inc | f8a2c4b7-a162-48ab-90b0-350e4da25c66 | 2025-12-16 | Warnings, Adverse reactions | 021SEF3731 |
| IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE | IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE | Ritedose Pharmaceuticals, LLC | e0dee492-8bf9-4360-be9b-9d6ee1ecb256 | 2025-12-10 | Warnings, Adverse reactions | 021SEF3731 |
| Ipratropium Bromide and Albuterol Sulfate | IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE | Chartwell RX, LLC | b444478a-10ce-484f-9039-6383dfb8161e | 2025-12-02 | Warnings, Adverse reactions | 021SEF3731 |
| Combivent Respimat | IPRATROPIUM BROMIDE AND ALBUTEROL | Boehringer Ingelheim Pharmaceuticals, Inc. | 9832312e-0310-4ab6-8501-afa976fc7eb2 | 2025-12-01 | Warnings, Adverse reactions | 021SEF3731 |
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | Bryant Ranch Prepack | 378461f2-7271-44a3-9da3-b39970b65d3a | 2025-11-10 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Nephron Pharmaceuticals Corporation | 574824f3-51cc-4b94-9c10-e3204d8b19f8 | 2025-11-07 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | ASCLEMED USA INC. | 8ea40065-4f59-434f-9ea1-7ef006fde66e | 2025-11-07 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Asclemed USA, Inc. | 056e145b-87aa-4009-a7ab-2ac0bd086eb0 | 2025-11-06 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | NuCare Pharmaceuticals, Inc. | 2c3f975c-dbd8-0362-e063-6394a90a16dd | 2025-10-21 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | NuCare Pharmaceuticals,Inc. | 4120061a-dbae-8918-e063-6394a90afbf2 | 2025-10-14 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Preferred Pharmaceuticals, Inc. | 081b7bbb-6692-4512-b135-863b73bf30a5 | 2025-10-13 | Warnings, Adverse reactions | 021SEF3731 |
| AIRSUPRA | ALBUTEROL SULFATE AND BUDESONIDE | AstraZeneca Pharmaceuticals LP | e60aa9f9-5139-44df-b886-ebddc3c7eb13 | 2025-09-18 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulate HFA | ALBUTEROL SULFATE | NuCare Pharmaceuticals,Inc. | 825975b1-a4a9-78ca-e053-2a91aa0a3948 | 2025-09-02 | Warnings, Adverse reactions | 021SEF3731 |
| ALBUTEROL SULFATE | ALBUTEROL SULFATE | QUAGEN PHARMACEUTICALS LLC | 99a490cc-e41d-436b-9cf3-8facb7ac714f | 2025-07-03 | Warnings, Adverse reactions | 021SEF3731 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.