NDC 0641-0376-21 - 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
- 0641-0376
- Requested NDC
- 0641-0376-21
- Package NDCs from labels
- 0641-0376-21, 0641-0376-25
- Manufacturer
- Sportpharm LLC
- Effective date
- 2026-07-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Diphenhydramine Hydrochloride - Sportpharm LLC | Sportpharm LLC | 2026-07-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride - Cardinal Health 107, LLC | Cardinal Health 107, LLC | 2026-05-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride - A-S Medication Solutions | A-S Medication Solutions | 2026-03-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride - A-S Medication Solutions | A-S Medication Solutions | 2026-02-11 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride Injection, USP Rx only | REMEDYREPACK INC. | 2026-01-14 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride Injection, USP Rx only | Henry Schein, Inc. | 2025-10-30 | HUMAN PRESCRIPTION DRUG LABEL |
| Deluxe Dental Emergency Kit - Best Dental Kit LLC | Best Dental Kit LLC | 2025-10-16 | HUMAN PRESCRIPTION DRUG LABEL |
| Basic Dental Emergency Kit - Best Dental Kit LLC | Best Dental Kit LLC | 2025-10-16 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride Injection, USP Rx only | Hikma Pharmaceuticals USA Inc. | 2024-04-09 | HUMAN PRESCRIPTION DRUG LABEL |
| DIPHENHYDRAMINE HYDROCHLORIDE - HF Acquisition Co. LLC, DBA Health First | HF Acquisition Co. LLC, DBA Health First | 2024-02-22 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride - Medical Purchasing Solutions, LLC | Medical Purchasing Solutions, LLC | 2023-04-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride - General Injectables & Vaccines, Inc | General Injectables & Vaccines, Inc | 2022-12-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Sodium Chloride - Aerospace Accessory Service, Inc | Aerospace Accessory Service, Inc | 2021-05-18 | MEDICAL DEVICE |
| Model AA-8565CV-ACT Model AA-8565CV - Aerospace Accessory Service, Inc | Aerospace Accessory Service, Inc | 2021-05-18 | MEDICAL DEVICE |
| Diphenhydramine Hydrochloride - Sina Health Inc | Sina Health Inc | 2019-02-04 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride Injection, USP Rx only | NuCare Pharmaceuticals,Inc. | 2017-12-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride - Rebel Distributors Corp | Rebel Distributors Corp | 2012-03-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride Injection, USP Rx only | Dispensing Solutions, Inc. | 2011-10-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Diphenhydramine Hydrochloride - TYA Pharmaceuticals | TYA Pharmaceuticals | 2011-06-13 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0641-0376-21 | Diphenhydramine Hydrochloride | 1 mL in 1 VIAL | INJECTION | 1 | 12 | |
| 0641-0376-25 | Diphenhydramine Hydrochloride | 25 in 1 PACKAGE | INJECTION | 25 | 12 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0641-0376-21 | ML - Milliliter | 0641-0376 | 8c8139e5-8f02-4c81-87c2-2d319fdbd594 | 1 | 2012-07-24 |
| 0641-0376-25 | ML - Milliliter | 0641-0376 | a1a960fe-d7c4-417f-91de-2ef619a68ff9 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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.