NDC 51672-1360-01 - Acyclovir
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
- 51672-1360
- Requested NDC
- 51672-1360-01
- Package NDCs from labels
- 51672-1360-1, 51672-1360-2, 51672-1360-5, 51672-1360-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2025-09-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Acyclovir Ointment USP, 5% | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-09-29 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-1360-1 | Acyclovir | 15 g in 1 TUBE | OINTMENT | 15 | 5 | |
| 51672-1360-1 | Acyclovir | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-1360-2 | Acyclovir | 30 g in 1 TUBE | OINTMENT | 30 | 5 | |
| 51672-1360-2 | Acyclovir | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-1360-5 | Acyclovir | 1 in 1 CARTON | OINTMENT | 1 | 5 | |
| 51672-1360-5 | Acyclovir | 5 g in 1 TUBE | OINTMENT | 5 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-1360 | ACYCLOVIR OINTMENT [SUN PHARMACEUTICAL INDUSTRIES, INC.] | 3 | Current NDC, Legacy NDC, 6 package rows | 20250406_962b2e1a-ba9d-4b39-b6d1-203947166482.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-1360-1 | GM - Gram | 51672-1360 | 03d1dfa6-12c1-4688-8c5e-6082116aa76f | 1 | 2017-03-06 |
| 51672-1360-2 | GM - Gram | 51672-1360 | 3ab83581-69ee-40d4-bb74-dd7af371494a | 1 | 2017-03-06 |
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 |
|---|---|---|---|---|---|---|
| Acyclovir | ACYCLOVIR | ACTAVIS PHARMA, INC. | b360a808-a24d-4f3c-89a7-9941422d17d6 | 2020-10-31 | Warnings, Adverse reactions | 197312 X4HES1O11F |
| Zovirax | ACYCLOVIR | Bausch Health US, LLC | 50278e0e-da1e-45ee-9fcb-672b2a219911 | 2020-10-31 | Warnings, Adverse reactions | 197312 X4HES1O11F |
| acyclovir | ACYCLOVIR | Asclemed USA, Inc. | e186fdc9-b60e-4280-8d60-36cae9f2838f | 2020-09-25 | Warnings, Adverse reactions | X4HES1O11F |
| Xerese | ACYCLOVIR AND HYDROCORTISONE | Bausch Health US LLC | 3b6ac164-0f1e-4f36-94a1-1fdb07d710f5 | 2020-08-03 | Warnings, Adverse reactions | X4HES1O11F |
| acyclovir | ACYCLOVIR | Proficient Rx LP | 51052f0e-1a07-405a-a962-981ce9439e02 | 2020-02-01 | Warnings, Adverse reactions | X4HES1O11F |
| Acyclovir | ACYCLOVIR | Xiromed, LLC | 3e222423-3bf2-6584-6d54-447b1b26dc42 | 2020-01-30 | Warnings, Adverse reactions | 197312 X4HES1O11F |
| Acyclovir | ACYCLOVIR | Proficient Rx LP | 6714cfd9-97d3-4290-b618-54594d89cf4e | 2020-01-01 | Warnings, Adverse reactions | X4HES1O11F |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.