NDC 68084-949-95 - 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
- 68084-949
- Requested NDC
- 68084-949-95
- Package NDCs from labels
- 68084-949-95, 68084-949-25
- 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 |
|---|---|---|---|---|---|---|
| 68084-949-25 | Albuterol Sulfate | 30 in 1 BOX, UNIT-DOSE | TABLET | 30 | 5 | |
| 68084-949-95 | 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 |
|---|---|---|---|---|---|
| 68084-949-25 | EA - Each | 68084-949 | eca9a593-f617-4c87-8c9a-50d7a6b4dca3 | 1 | 2015-10-02 |
| 68084-949-95 | EA - Each | 68084-949 | b222496d-8c4d-4f4a-85c2-3bd2037c5fb0 | 1 | 2015-10-02 |
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 |
|---|---|---|---|---|---|---|
| Albuterol Sulfate | ALBUTEROL SULFATE | Sportpharm LLC | e31d8d13-ac19-4738-97d4-d7790ce2e8e3 | 2026-04-24 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol sulfate | ALBUTEROL SULFATE | Sportpharm LLC | 32d954ee-9790-4beb-95db-72dbf8efa639 | 2026-04-24 | Warnings, Adverse reactions | 021SEF3731 |
| Caldesene Baby | STARCH, CORN AND ZINC OXIDE | Insight Pharmaceuticals LLC | 9f12dee2-7afa-45e9-a729-0fd42bb77715 | 2026-04-22 | Warnings | O8232NY3SJ |
| Caldesene Medicated Protecting | CORNSTARCH AND ZINC OXIDE | Insight Pharmaceuticals LLC | ffc92a0f-a7cf-4a46-b2f1-089df2bbb96b | 2026-04-22 | Warnings | O8232NY3SJ |
| Albuterol Sulfate | ALBUTEROL SULFATE | Cardinal Health 107, LLC | d2132c1c-0f90-4c6f-afc0-f3814b6a7e5c | 2026-04-20 | Warnings, Adverse reactions | 021SEF3731 |
| albuterol sulfate | ALBUTEROL SULFATE | Golden State Medical Supply, Inc. | a22af54a-c010-ab8b-e053-2a95a90a8862 | 2026-04-15 | Warnings, Adverse reactions | ANDA072637 197316 197318 021SEF3731 |
| Albuterol | ALBUTEROL | Amneal Pharmaceuticals NY LLC | 230d66fc-f62c-42a6-adb3-0a0f879c8ad4 | 2026-04-14 | Warnings, Adverse reactions | 197316 197318 021SEF3731 |
| Albuterol sulfate | ALBUTEROL SULFATE | REMEDYREPACK INC. | 0cfb6c5d-eac2-4a1c-8a0f-6b00e819adda | 2026-04-13 | Warnings, Adverse reactions | 021SEF3731 |
| Ipratropium Bromide and Albuterol Sulfate | IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE | Sun Pharmaceutical Industries, Inc. | 38f9a201-3954-4370-8e71-7ec2df88a1ff | 2026-04-09 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Sun Pharmaceutical Industries, Inc. | bb538b7d-e390-419a-9404-a57c1db4a447 | 2026-04-09 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Cardinal Health 107, LLC | 6ec88f64-66a2-4ca9-9913-c192fc33f88b | 2026-04-08 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Nephron Pharmaceuticals Corporation | 285a656c-f77f-4e77-b0a8-a0e9c901803f | 2026-04-06 | Warnings, Adverse reactions | 021SEF3731 |
| albuterol sulfate | ALBUTEROL SULFATE | Sun Pharmaceutical Industries, Inc. | 87b8cd3c-2849-4b50-b63e-9ea379165c07 | 2026-03-16 | Warnings, Adverse reactions | ANDA072637 53489-176 53489-177 197316 197318 4d289f6d-634d-2125-e063-6394a90aa25d 87b8cd3c-2849-4b50-b63e-9ea379165c07 021SEF3731 |
| Albuterol | ALBUTEROL | Mylan Pharmaceuticals Inc. | 9e6e982b-7dfe-45b8-aa76-754e8d2a8ef6 | 2026-03-15 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Preferred Pharmaceuticals Inc. | c90e80b2-882e-4c0c-bfac-d67eb1da724d | 2026-02-16 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Mylan Pharmaceuticals Inc. | 5329614f-ae0b-4854-bb6f-ea0b7dae87c0 | 2026-02-10 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulate HFA | ALBUTEROL SULFATE | REMEDYREPACK INC. | 77d34a3c-ccc6-420a-ad31-a1af55f7de76 | 2026-01-30 | Warnings, Adverse reactions | 021SEF3731 |
| IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE | IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE | Golden State Medical Supply, Inc. | 2ebc820b-a423-46ef-8eba-9fbc93daff44 | 2026-01-28 | Warnings, Adverse reactions | 021SEF3731 |
| Albuterol Sulfate | ALBUTEROL SULFATE | Preferred Pharmaceuticals Inc. | 1f0bf143-66d4-4a39-b2d1-a5c460ffdcf9 | 2026-01-22 | Warnings, Adverse reactions | 021SEF3731 |
| VENTOLIN HFA | ALBUTEROL SULFATE | REMEDYREPACK INC. | 2ed73618-be3a-4331-9509-6401258f791f | 2026-01-19 | Warnings, Adverse reactions | 021SEF3731 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.