NDC 72205-014-11 - Pregabalin
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
- 72205-014
- Requested NDC
- 72205-014-11
- Package NDCs from labels
- 72205-014-90, 72205-014-99, 72205-014-11, 72205-014-06
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-07-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Pregabalin - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-07-28 | HUMAN PRESCRIPTION DRUG LABEL |
| Pregabalin - ST. MARY'S MEDICAL PARK PHARMACY | ST. MARY'S MEDICAL PARK PHARMACY | 2026-02-24 | HUMAN PRESCRIPTION DRUG LABEL |
| Pregabalin - A-S Medication Solutions | A-S Medication Solutions | 2026-02-08 | Human Prescription Drug Label |
| Pregabalin - Proficient Rx LP | Proficient Rx LP | 2025-10-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Pregabalin | Novadoz Pharmaceuticals LLC | MSN LABORATORIES PRIVATE LIMITED | MSN Pharmaceuticals Inc. | 2025-08-28 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72205-014-06 | Pregabalin | 100 in 1 CARTON | CAPSULE | 100 | 6 | |
| 72205-014-11 | Pregabalin | 10 in 1 BLISTER PACK | CAPSULE | 10 | 6 | |
| 72205-014-90 | Pregabalin | 90 in 1 BOTTLE | CAPSULE | 90 | 6 | |
| 72205-014-99 | Pregabalin | 1000 in 1 BOTTLE | CAPSULE | 1000 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72205-014-90 | EA - Each | 72205-014 | dd571995-3383-4864-91b4-595d39527a6e | 1 | 2019-08-06 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.