NDC 0093-2131-19 - Nitrofurantoin Macrocrystals
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
- 0093-2131
- Requested NDC
- 0093-2131-19
- Package NDCs from labels
- 0093-2131-19
- Manufacturer
- Liberty Pharmaceuticals, Inc.
- Effective date
- 2013-09-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| NITROFURANTOIN CAPSULES USP (Macrocrystals) Rx only 2130 2131 | Liberty Pharmaceuticals, Inc. | 2013-09-11 | HUMAN PRESCRIPTION DRUG LABEL |
| NITROFURANTOIN CAPSULES USP (Macrocrystals) Rx only 2130 2131 | Physicians Total Care, Inc. | 2012-04-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Nitrofurantoin Macrocrystals - Rebel Distributors Corp | Rebel Distributors Corp | 2011-12-20 | HUMAN PRESCRIPTION DRUG LABEL |
| NITROFURANTOIN CAPSULES USP (Macrocrystals) Rx only 2130 2131 | RedPharm Drug Inc. | TEVA Pharmaceutical Industries Ltd. | Barr Laboratories Inc. | 2011-06-22 | HUMAN PRESCRIPTION DRUG LABEL |
| NITROFURANTOIN CAPSULES USP (Macrocrystals) Rx only 2130 2131 | Blenheim Pharmacal, Inc. | 2011-06-07 | HUMAN PRESCRIPTION DRUG LABEL |
| NITROFURANTOIN MACROCRYSTALS - STAT RX USA LLC | STAT RX USA LLC | 2011-04-15 | 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 |
|---|---|---|---|---|---|
| 0093-2131-01 | EA - Each | 0093-2131 | 13fcb633-e735-4f8b-97ec-59808184298e | 1 | 2012-07-24 |
| 0093-2131-10 | EA - Each | 0093-2131 | 46762859-7906-466d-a149-0669e40b260c | 1 | 2012-07-24 |
| 0093-2131-19 | EA - Each | 0093-2131 | dfc92d82-9224-44ea-a77e-6a1661300434 | 1 | 2012-07-24 |
| 0093-2131-93 | EA - Each | 0093-2131 | d90ba0a0-33a1-483c-a74e-29c55a4e1e73 | 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.