NDC 71894-110 - Zolgensma
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
- 71894-110
- Package NDCs from labels
- 71894-110-01
- Manufacturer
- Novartis Innovative Technologies Inc.
- Effective date
- 2026-06-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Zolgensma - Novartis Innovative Technologies Inc. | Novartis Innovative Technologies Inc. | 2026-06-16 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 11.0 mL | 20000000000000 [arb'U] in 1mL | 14 |
| 71894-110-01 | Zolgensma | 5.5 mL in 1 VIAL | INJECTION, SUSPENSION | 5.5 mL | 20000000000000 [arb'U] in 1mL | 14 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Incontinence | ALOE, ARG. NIT., ARSENICUM ALB., BELLADONNA, BENZOICUM ACIDUM, BRYONIA, CANTHARIS, CAUSTICUM, EQUISETUM HYEMALE, FERRUM METALLICUM, GELSEMIUM, IGNATIA, KALI PHOS., LYCOPODIUM, NAT. MUR., NITRICUM AC., PLANTAGO, PULSATILLA, RHUS AROMATICA , SABAL, SECALE, SEPIA, STAPHYSAG.,STRAMONIUM, THYROIDINUM, VERBASCUM, ECHINACEA, HYDRASTIS | Newton Laboratories, Inc. | 9c0d8c82-6c4f-a511-e053-2995a90a793f | 2025-02-07 | Warnings | 451W47IQ8X |
| Isopropyl alcohol 70 percent | ISOPROPYL ALCOHOL | Good Sense (Geiss, Destin & Dunn, Inc.) | ac66be77-d358-44ea-8904-88186a7c2bbb | 2025-02-07 | Warnings | ND2M416302 |
| Rubbing Alcohol 70 Percent Isopropyl | ISOPROPYL ALCOHOL | Harris Teeter, LLC | 4196dd97-9041-4712-8196-02237a3b0cb2 | 2025-02-07 | Warnings | ND2M416302 |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | Harris Teeter, LLC | 1b044f47-45e1-40a3-81b0-2717ed425f16 | 2025-02-07 | Warnings | ND2M416302 |
| Dairy-Grain-Nightshades | IRIS VERS., SOLIDAGO, ANTIMON. CRUD., ARG. NIT., ARSENICUM ALB., AVENA, BAPTISIA, BELLADONNA, BRYONIA, CAPSICUM, CARDUUS BEN., CINCHONA, DULCAMARA, FAGOPYRUM, GELSEMIUM, HYOSCYAMUS, IPECAC., LAC VAC., LACHESIS, LYCOPODIUM, NAT. MUR., PHOS., PODOPH. PELT., PULSATILLA, RHUS TOX., SAC. LAC., SECALE, SEPIA, STRAMONIUM, TABACUM, TRITICUM, USTILAGO MAIDIS, VERBASCUM, LYCOPERSICUM, SOLANUM NIG., SOLANUM TUB., STIGMATA, TORULA CEREVISIAE. | Newton Laboratories, Inc. | 9ba83c60-35be-181a-e053-2a95a90a9895 | 2025-02-06 | Warnings | 451W47IQ8X |
| 4 Kids Cold and Cough Nighttime | ONION, CALCIUM SULFIDE, SODIUM CHLORIDE, ANEMONE PULSATILLA, ARABICA COFFEE BEAN, MATRICARIA CHAMOMILLA, SULFUR, PHOSPHORUS AND GOLDENSEAL | Hyland's Consumer Health Inc. | 71e93027-33c9-6147-e053-2a95a90aaa09 | 2025-02-06 | Warnings | 451W47IQ8X |
| Isopropyl alcohol 70 percent Wintergreen | ISOPROPYL ALCOHOL | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | 444cd7f4-cf61-49b6-a93e-915d250838da | 2025-02-06 | Warnings | ND2M416302 |
| HULIO | ADALIMUMAB-FKJP | Biocon Biologics Inc | 661ad70b-c313-2899-8a7e-7a67bd897ca9 | 2025-02-06 | Boxed warning, Warnings, Adverse reactions | 797544 |
| Isopropyl alcohol 91 percent | ISOPROPYL ALCOHOL | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 444883fc-7ae4-4dd3-bd2b-f94c3265c170 | 2025-02-05 | Warnings | ND2M416302 |
| PHARMACIST CHOICE ALCOHOL STERILE PREP PAD | ISOPROPYL ALCOHOL | Simple Diagnostics | 0fc4a4b2-342b-5948-e054-00144ff88e88 | 2025-02-04 | Warnings | 797544 ND2M416302 |
| Jacksons Cell Salts 12 IN 1 | CALC FLUOR, CALC PHOS, CALC SULPH, FERRUM PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT MUR, NAT PHOS, NAT SULPH, SILICEA | Zettl Health Inc. | 25ba49d0-0369-3666-e063-6294a90a71c4 | 2025-02-04 | 451W47IQ8X | |
| Well at Walgreens | SODIUM BICARBONATE, SODIUM CHLORIDE | Walgreen Company | cb5d3d9d-2481-4303-b6af-0002de8c9065 | 2025-01-31 | Warnings | 451W47IQ8X |
| Sinus Wash Packet | SODIUM BICARBONATE, SODIUM CHLORIDE | RITE AID CORPORATION | d5b44ae7-81e8-1413-e053-2995a90a5933 | 2025-01-31 | Warnings | 451W47IQ8X |
| Sinus Wash Saline Refills Meijer | SODIUM BICARBONATE, SODIUM CHLORIDE | Meijer, Inc. | dd7465fe-503a-4e34-e053-2995a90a2778 | 2025-01-31 | Warnings | 451W47IQ8X |
| SinuCleanse | SODIUM BICARBONATE, SODIUM CHLORIDE | ASCENT CONSUMER PRODUCTS, INC. | ff4df6c5-c85f-406a-89d7-8c2853fd5e10 | 2025-01-31 | Warnings | 451W47IQ8X |
| CVS | SODIUM BICARBONATE, SODIUM CHLORIDE | CVS Pharmacy | bccefef8-f92d-42fc-90fc-86644d1df655 | 2025-01-31 | Warnings | 451W47IQ8X |
| Well at Walgreens | SODIUM BICARBONATE, SODIUM CHLORIDE | Walgreen Company | bcd336b4-9189-44d5-ae6d-81e535eff6b5 | 2025-01-31 | Warnings | 451W47IQ8X |
| SinuCleanse | SODIUM BICARBONATE, SODIUM CHLORIDE | ASCENT CONSUMER PRODUCTS, INC. | c33bf872-54aa-45e0-9e40-a6565a13f198 | 2025-01-31 | Warnings | 451W47IQ8X |
| Sodium Chloride Normal Salt | SODIUM CHLORIDE | Citragen Pharmaceuticals Inc | aae783b2-18fe-69ca-e053-2a95a90a0800 | 2025-01-30 | Warnings | 451W47IQ8X |
| Sodium Chloride Normal Salt | SODIUM CHLORIDE | Citragen Pharmaceuticals Inc | 82c29f1d-a018-7483-e053-2a91aa0a8f7e | 2025-01-30 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.