NDC 0955-2900-01 - Insulin glargine U-300
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
- 0955-2900
- Requested NDC
- 0955-2900-01
- Package NDCs from labels
- 0955-2900-01, 0955-2900-02
- Manufacturer
- Sanofi-Aventis U.S. LLC | Genzyme Corporation | Sanofi-Aventis Deutschland GmbH
- Effective date
- 2025-05-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Insulin glargine U-300 - Sanofi-Aventis U.S. LLC | Genzyme Corporation | Sanofi-Aventis Deutschland GmbH | Sanofi-Aventis U.S. LLC | Genzyme Corporation | Sanofi-Aventis Deutschland GmbH | 2025-05-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0955-2900-01 | Insulin glargine U-300 Max | 3 mL in 1 SYRINGE | INJECTION, SOLUTION | 3 | 7 | |
| 0955-2900-02 | Insulin glargine U-300 Max | 2 in 1 CARTON | INJECTION, SOLUTION | 2 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0955-2900 | INSULIN GLARGINE U-300 (INSULIN GLARGINE) INJECTION, SOLUTION INSULIN GLARGINE U-300 MAX (INSULIN GLARGINE) INJECTION, SOLUTION [WINTHROP U.S.] | 6 | Current NDC, 2 package rows | 20240913_99ea856d-9562-443a-9422-1006a3cff2f4.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0955-2900-01 | ML - Milliliter | 0955-2900 | d5f1116f-3b0d-4a22-b902-789dc1133f55 | 1 | 2024-02-14 |
| 0955-2900-02 | ML - Milliliter | 0955-2900 | 6dda0158-cc5b-4530-884a-73ea65000a7e | 1 | 2024-02-14 |
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.
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| Plus Rinse Emergency Eyewash | PURIFIED WATER | INNOVATIVE SAFETY SUPPLY INC. | b3f47d26-39e4-4aea-bb92-358def52b652 | 2026-01-08 | Warnings | 059QF0KO0R |
| pH Neutral Emergency Eyewash | WATER | INNOVATIVE SAFETY SUPPLY INC. | 29a1bd1e-d0dd-478f-e063-6394a90ab0aa | 2026-01-08 | Warnings | 059QF0KO0R |
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| Male Endocrine Axis Drops 5019 | MALE ENDOCRINE AXIS DROPS | Professional Complementary Health Formulas | 607dd42d-5b41-4c0a-8499-83763dc04ad1 | 2026-01-08 | Warnings | J41CSQ7QDS |
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| Libido Stim Liquescence 3014 | LIBIDO STIM LIQUESCENCE | Professional Complementary Health Formulas | 3d59b77d-817b-4021-a6dd-75d3b4b60866 | 2026-01-08 | Warnings | PDC6A3C0OX |
| Insulin 1556 | INSULIN | Professional Complementary Health Formulas | 88170080-374d-456e-90bc-48e873878ce7 | 2026-01-08 | Warnings | 2ZM8CX04RZ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.