NDC 70710-1641-06 - Lubiprostone
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
- 70710-1641
- Requested NDC
- 70710-1641-06
- Package NDCs from labels
- 70710-1641-6, 70710-1641-1, 70710-1641-06
- Manufacturer
- Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM
- Effective date
- 2025-02-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lubiprostone - Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-02-06 | HUMAN PRESCRIPTION DRUG LABEL |
| Lubiprostone - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2023-03-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1641-1 | Lubiprostone | 100 in 1 BOTTLE | CAPSULE | 100 | 1 | |
| 70710-1641-6 | Lubiprostone | 60 in 1 BOTTLE | CAPSULE | 60 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1641 | LUBIPROSTONE CAPSULE [ZYDUS PHARMACEUTICALS USA INC.] | 1 | Current NDC, 2 package rows | 20230328_6c11a204-6831-4269-a3c4-1702ed83f74b.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1641-6 | EA - Each | 70710-1641 | 79a1fbe8-ccab-408f-a0af-228071c2b415 | 1 | 2023-12-05 |
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 |
|---|---|---|---|---|---|---|
| Nuance Salma Hayek Renewed Radiance Brightening BB Cream Broad Spectrum SPF 30 Sunscreen | NUANCE SALMA HAYEK RENEWED RADIANCE BRIGHTENING BB CREAM BROAD SPECTRUM SPF 30 SUNSCREEN | Mana Products | d0e00d97-dbf4-46af-aeda-bdfd6f49b5ab | 2016-09-08 | Warnings | 15FIX9V2JP |
| 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 |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| 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 |
| 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 |
| 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.