NDC 0093-8940-19 - 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
- 0093-8940
- Requested NDC
- 0093-8940-19
- Package NDCs from labels
- 0093-8940-01, 0093-8940-05, 0093-8940-19, 0093-8940-93
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2021-04-23
- 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 | 2021-04-23 | HUMAN PRESCRIPTION DRUG LABEL |
| ACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP 8940 8943 8947 Rx only | REMEDYREPACK INC. | 2020-04-07 | HUMAN PRESCRIPTION DRUG LABEL |
| Acyclovir - RedPharm Drug, Inc. | RedPharm Drug, Inc. | 2020-01-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Acyclovir - Proficient Rx LP | Proficient Rx LP | 2019-12-01 | HUMAN PRESCRIPTION DRUG LABEL |
| ACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP 8940 8943 8947 Rx only | Teva Pharmaceuticals USA, Inc. | 2014-09-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Acyclovir - Bryant Ranch Prepack | Bryant Ranch Prepack | 2014-07-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Acyclovir - Aidarex Pharmaceuticals LLC | Aidarex Pharmaceuticals LLC | 2012-09-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Acyclovir - H.J. Harkins Company, Inc. | Teva Pharmaceuticals USA Inc | H.J. Harkins Company, Inc. | Teva Pharmaceuticals USA Inc | 2011-10-27 | HUMAN PRESCRIPTION DRUG LABEL |
| ACYCLOVIR CAPSULES USP ACYCLOVIR TABLETS USP 8940 8943 8947 Rx only | Blenheim Pharmacal, Inc. | 2011-04-29 | 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 Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0093-8940-01 | EA - Each | 0093-8940 | e9db9442-cc0a-406b-a617-bcb228afa229 | 1 | 2012-07-24 |
| 0093-8940-05 | EA - Each | 0093-8940 | a2752213-2b9e-44cb-8b17-895ec72b3867 | 1 | 2012-07-24 |
| 0093-8940-19 | EA - Each | 0093-8940 | 41e1f211-46c2-494b-9425-405c58e7b2e1 | 1 | 2012-07-24 |
| 0093-8940-93 | EA - Each | 0093-8940 | 7d4cf114-2b25-4b1c-b396-238696497409 | 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.