NDC 72162-1908-07 - 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
- 72162-1908
- Requested NDC
- 72162-1908-07
- Package NDCs from labels
- 72162-1908-1, 72162-1908-2, 72162-1908-3, 72162-1908-4, 72162-1908-5, 72162-1908-6, 72162-1908-7, 72162-1908-8, 72162-1908-9, 72162-1908-0, 72162-1908-07
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2023-05-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Acyclovir - Bryant Ranch Prepack | Bryant Ranch Prepack | 2023-05-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72162-1908-0 | Acyclovir | 30 in 1 BOTTLE | CAPSULE | 30 | 100 | |
| 72162-1908-1 | Acyclovir | 25 in 1 BOTTLE | CAPSULE | 25 | 100 | |
| 72162-1908-2 | Acyclovir | 35 in 1 BOTTLE | CAPSULE | 35 | 100 | |
| 72162-1908-3 | Acyclovir | 50 in 1 BOTTLE | CAPSULE | 50 | 100 | |
| 72162-1908-4 | Acyclovir | 100 in 1 BOTTLE | CAPSULE | 100 | 100 | |
| 72162-1908-5 | Acyclovir | 40 in 1 BOTTLE | CAPSULE | 40 | 100 | |
| 72162-1908-6 | Acyclovir | 60 in 1 BOTTLE | CAPSULE | 60 | 100 | |
| 72162-1908-7 | Acyclovir | 120 in 1 BOTTLE | CAPSULE | 120 | 100 | |
| 72162-1908-8 | Acyclovir | 20 in 1 BOTTLE | CAPSULE | 20 | 100 | |
| 72162-1908-9 | Acyclovir | 90 in 1 BOTTLE | CAPSULE | 90 | 100 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72162-1908 | ACYCLOVIR CAPSULE [BRYANT RANCH PREPACK] | 100 | Current NDC, 10 package rows | 20230511_e8433261-07f1-448b-aaf4-631414598c08.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72162-1908-0 | EA - Each | 72162-1908 | 6353a4e2-cb80-4423-87ee-7319f7671fc3 | 1 | 2023-10-16 |
| 72162-1908-1 | EA - Each | 72162-1908 | be8eaa11-215b-480e-b22a-64b02b7b34df | 1 | 2023-10-16 |
| 72162-1908-2 | EA - Each | 72162-1908 | 7df3dd42-9854-46c4-877c-c5d4f0de9e01 | 1 | 2023-10-16 |
| 72162-1908-3 | EA - Each | 72162-1908 | 24daa4de-2ccf-42c0-bcca-5bd91cd350b0 | 1 | 2023-10-16 |
| 72162-1908-4 | EA - Each | 72162-1908 | 4c489749-10cc-4fe9-9f39-cf458e7663c9 | 1 | 2023-10-16 |
| 72162-1908-5 | EA - Each | 72162-1908 | 0db7e27e-441e-4227-a0ff-8e8468ff61c9 | 1 | 2023-10-16 |
| 72162-1908-6 | EA - Each | 72162-1908 | bde3759c-50f8-4073-a761-653eb901a960 | 1 | 2023-10-16 |
| 72162-1908-7 | EA - Each | 72162-1908 | 56636673-2517-40a6-9b2e-a5500fbc24c3 | 1 | 2023-10-16 |
| 72162-1908-8 | EA - Each | 72162-1908 | 5db50785-b310-4c16-a2ff-ccc86a772101 | 1 | 2023-10-16 |
| 72162-1908-9 | EA - Each | 72162-1908 | 49387dfb-9d24-4377-b1c4-a1c481705253 | 1 | 2023-10-16 |
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.
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| e l f Camo Semi Matte CC SPF 30 Light 240 W | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | 8c12a34c-f648-4b55-8265-d430c72ae205 | 2025-10-31 | Warnings | 15FIX9V2JP |
| e l f Camo Semi Matte CC SPF 30 Light 250 W | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | 0b1c20e6-9d98-4b69-8fe0-ac5e9f2b9b2c | 2025-10-31 | Warnings | 15FIX9V2JP |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.