NDC 70710-1591-01 - acetazolamide
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
- 70710-1591
- Requested NDC
- 70710-1591-01
- Package NDCs from labels
- 70710-1591-3, 70710-1591-9, 70710-1591-1, 70710-1591-5, 70710-1591-0, 70710-1591-4, 70710-1591-01
- Manufacturer
- American Health Packaging
- Effective date
- 2025-05-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| acetazolamide - American Health Packaging | American Health Packaging | 2025-05-30 | HUMAN PRESCRIPTION DRUG LABEL |
| acetazolamide - Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Limited | 2024-10-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1591-0 | acetazolamide | 1000 in 1 BOTTLE | CAPSULE | 1000 | 8 | |
| 70710-1591-1 | acetazolamide | 100 in 1 BOTTLE | CAPSULE | 100 | 8 | |
| 70710-1591-3 | acetazolamide | 30 in 1 BOTTLE | CAPSULE | 30 | 8 | |
| 70710-1591-4 | acetazolamide | 10 in 1 BLISTER PACK | CAPSULE | 10 | 8 | |
| 70710-1591-4 | acetazolamide | 10 in 1 CARTON | CAPSULE | 10 | 8 | |
| 70710-1591-5 | acetazolamide | 500 in 1 BOTTLE | CAPSULE | 500 | 8 | |
| 70710-1591-9 | acetazolamide | 90 in 1 BOTTLE | CAPSULE | 90 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1591 | ACETAZOLAMIDE CAPSULE [ZYDUS PHARMACEUTICALS (USA) INC.] | 8 | Current NDC, Legacy NDC, 7 package rows | 20241012_bf514e99-4958-44a0-a87a-02a950f87e60.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1591-1 | EA - Each | 70710-1591 | 55671302-c3bc-46f9-8d04-26bde539c170 | 1 | 2020-04-20 |
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 |
|---|---|---|---|---|---|---|
| Meijer Kids Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distribution, Inc. | 7415511e-1ecf-4646-b64b-267fbf7d116b | 2016-06-02 | Warnings | 15FIX9V2JP |
| Meijer Baby Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distributing Inc. | 2434de23-bcc9-4a83-9945-16fc3f2b8c61 | 2016-06-01 | Warnings | 15FIX9V2JP |
| TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 6a996e03-907f-4e6a-b232-0892b86956b0 | 2015-08-21 | Warnings | 15FIX9V2JP |
| CVS Hand Sanitizer | ALCOHOL | CVS | d0081c50-c0d2-436a-ba83-5d1982ae64b7 | 2015-08-17 | Warnings | 3K9958V90M |
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| Instant Hand Sanitizer | ALCOHOL | Safetec of America, Inc. | f9e30645-491b-4f54-acfd-f863ee235607 | 2013-08-07 | Warnings | 3K9958V90M |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.