NDC 42023-216-01 - Ephedrine 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
- 42023-216
- Requested NDC
- 42023-216-01
- Package NDCs from labels
- 42023-216-01, 42023-216-25, 42023-216-83
- Manufacturer
- Par Health USA, LLC
- Effective date
- 2026-03-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ephedrine Sulfate - Par Health USA, LLC | Par Health USA, LLC | 2026-03-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Ephedrine Sulfate - Par Health USA, LLC | Endo USA, Inc. | Par Health USA, LLC | Endo USA, Inc. | 2026-01-21 | HUMAN PRESCRIPTION DRUG LABEL |
| EPHEDRINE SULFATE - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2024-02-26 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42023-216-01 | Ephedrine Sulfate | 1 mL in 1 VIAL | INJECTION, SOLUTION | 1 | 10 | |
| 42023-216-25 | Ephedrine Sulfate | 25 in 1 CARTON | INJECTION, SOLUTION | 25 | 10 | |
| 42023-216-83 | Ephedrine Sulfate | 25 in 1 CARTON | INJECTION, SOLUTION | 25 | 7 | |
| 42023-216-83 | Ephedrine Sulfate | 1 mL in 1 VIAL | INJECTION, SOLUTION | 1 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 42023-216 | EPHEDRINE SULFATE INJECTION, SOLUTION [ENDO USA, INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20240425_38723cb3-dfca-4c81-8c6f-63dd99929191.zip |
| 42023-216 | EPHEDRINE SULFATE INJECTION, SOLUTION [ENDO USA, INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241018_3e43cc8e-bf4e-44ef-a07d-4336367b9bdb.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 42023-216-01 | ML - Milliliter | 42023-216 | 6a623ae7-d3f7-4b38-9ca4-a934b31c73fb | 1 | 2017-03-06 |
| 42023-216-25 | ML - Milliliter | 42023-216 | f9d3f2b5-4cc7-44a5-b8eb-e59ce354842b | 1 | 2017-03-06 |
| 42023-216-83 | ML - Milliliter | 42023-216 | 7189d2c8-1205-4d57-9be4-e8d300505cfc | 1 | 2018-07-03 |
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 |
|---|---|---|---|---|---|---|
| KUGIG ALOE FOAMING INTIMATE WASH | INTIMATE CLEANSING FOAM | Hong Kong KangXing Centennial Management Limited | 59f4d398-1186-a168-e063-6294a90ab44b | 2026-08-26 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | REMEDYREPACK INC. | 5dd5d148-6e23-41de-bff5-551b2aea9598 | 2026-08-24 | Warnings, Adverse reactions | 059QF0KO0R |
| BM BM63 DROPS | CEANOTHUS, KALI ARSEN, KALI MUR, SELENIUM, THALLIUM, WIESBADEN | BM Private Limited | 59006d82-610a-2e08-e063-6394a90af1ed | 2026-08-14 | Warnings | 059QF0KO0R |
| Ephedrine Sulfate | EPHEDRINE SULFATE | Medical Purchasing Solutions, LLC | d89dd8d5-7698-61db-e053-2a95a90a764b | 2026-08-10 | Warnings, Adverse reactions | 1116294 U6X61U5ZEG |
| Sterile Water | WATER | Cardinal Health 107, LLC | 48d75a7c-8329-48a8-bea0-a8c144ddf637 | 2026-08-07 | Warnings, Adverse reactions | 059QF0KO0R |
| Garzulys | INSULIN ASPART-FSAN | Meitheal Pharmaceuticals Inc. | 30c64769-d2f7-4604-ac9e-2a6bc09506c9 | 2026-07-31 | Warnings, Adverse reactions | 059QF0KO0R |
| DECONIMO Reconstitution | DECONIMO RECONSTITUTION | Image Amazon LLC | 57ab9b1c-9a18-3786-e063-6394a90a2c63 | 2026-07-28 | Warnings | 059QF0KO0R |
| Ephedrine Sulfate | EPHEDRINE SULFATE | Medical Purchasing Solutions, LLC | 57b49792-7ea1-c5cc-e063-6394a90a5b2b | 2026-07-28 | Warnings, Adverse reactions | 1116294 U6X61U5ZEG |
| Sterile Water | WATER | Cardinal Health 107, LLC | 9655cd02-82b5-4a75-813b-854b19551481 | 2026-07-21 | Warnings, Adverse reactions | 059QF0KO0R |
| Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g) | NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE) | Reedfresh Co., LTD | 55d703ca-ff9d-0dbc-e063-6294a90ab6b1 | 2026-07-05 | Warnings | 059QF0KO0R |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Protective Industrial Products, Inc. | 558e5926-9027-d3f6-e063-6294a90ab121 | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 2000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a1d07e-0006-0c75-e063-6394a90a7acc | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
| Remodulin | TREPROSTINIL | United Therapeutics Corporation | 6c80bb38-e8db-4138-9f0d-dbbf9c673185 | 2026-07-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Fendall 2000 Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37dead3e-60cb-88ae-e063-6294a90a8f70 | 2026-06-24 | Warnings | 059QF0KO0R |
| Bacteriostatic Water | BACTERIOSTATIC WATER | Fujian Genohope Biotech Ltd. | 54f66b82-c9e5-a2bc-e063-6394a90adbbc | 2026-06-23 | 059QF0KO0R | |
| Humalog | INSULIN LISPRO | Eli Lilly and Company | c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f | 2026-06-16 | Warnings, Adverse reactions | 059QF0KO0R |
| BM BM70 DROPS | ANTIM CURD, FERR MET, PHOSPHORUS, SULPHUR, WIESBADEN, THUJA, VERATRUM ALB | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 54113d1f-e8e7-6b4c-e063-6394a90a0edf | 2026-06-12 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.