NDC 72485-101-01 - Diphenhydramine Hydrochloride
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
- 72485-101
- Requested NDC
- 72485-101-01
- Package NDCs from labels
- 72485-101-01, 72485-101-25, 72485-101-05
- Manufacturer
- ProPharma Distribution
- Effective date
- 2025-12-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diphenhydramine Hydrochloride - ProPharma Distribution | ProPharma Distribution | 2025-12-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride Injection, USP | REMEDYREPACK INC. | 2024-03-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride Injection, USP | Armas Pharmaceuticals Inc. | 2023-07-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride - Medical Purchasing Solutions, LLC | Medical Purchasing Solutions, LLC | 2023-04-26 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72485-101-01 | Diphenhydramine Hydrochloride | 1 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 1 | 4 | |
| 72485-101-05 | Diphenhydramine Hydrochloride | 5 in 1 CARTON | INJECTION, SOLUTION | 5 | 4 | |
| 72485-101-25 | Diphenhydramine Hydrochloride | 25 in 1 CARTON | INJECTION, SOLUTION | 25 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72485-101-01 | ML - Milliliter | 72485-101 | 8d6392e5-dedb-4e32-9a4a-9b86c9a27dee | 1 | 2019-06-19 |
| 72485-101-05 | ML - Milliliter | 72485-101 | 5476ad9c-3fc6-46b2-8059-545e2eae8430 | 1 | 2023-06-06 |
| 72485-101-25 | ML - Milliliter | 72485-101 | f341cc59-8aa3-4145-be86-4cfb8b9f1961 | 1 | 2019-06-19 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.