NDC 0591-0727 - Meperidine HCl
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
- 0591-0727
- Package NDCs from labels
- 0591-0727-01
- Manufacturer
- Watson Laboratories, Inc.
- Effective date
- 2007-03-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Meperidine HCl - Watson Laboratories, Inc. | Watson Laboratories, Inc. | 2007-03-30 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0591-0727-01 | Meperidine HCl | 100 in 1 BOTTLE | TABLET | 100 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Meperidine hydrochloride | ACTIVE INGREDIENT | N8E7F7Q170 | MEPERIDINE HCL (MEPERIDINE HYDROCHLORIDE) TABLET [WATSON LABORATORIES, INC.] | 1 | |
| Meperidine | ACTIVE MOIETY | 9E338QE28F | MEPERIDINE HCL (MEPERIDINE HYDROCHLORIDE) TABLET [WATSON LABORATORIES, INC.] | 1 | |
| confectioners sugar | INACTIVE INGREDIENT | MEPERIDINE HCL (MEPERIDINE HYDROCHLORIDE) TABLET [WATSON LABORATORIES, INC.] | 1 | ||
| lactose monohydrate | INACTIVE INGREDIENT | MEPERIDINE HCL (MEPERIDINE HYDROCHLORIDE) TABLET [WATSON LABORATORIES, INC.] | 1 | ||
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | MEPERIDINE HCL (MEPERIDINE HYDROCHLORIDE) TABLET [WATSON LABORATORIES, INC.] | 1 | |
| povidone | INACTIVE INGREDIENT | MEPERIDINE HCL (MEPERIDINE HYDROCHLORIDE) TABLET [WATSON LABORATORIES, INC.] | 1 | ||
| sodium starch glycolate | INACTIVE INGREDIENT | MEPERIDINE HCL (MEPERIDINE HYDROCHLORIDE) TABLET [WATSON LABORATORIES, INC.] | 1 |
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 |
|---|---|---|---|---|---|---|
| Meperidine Hydrochloride | MEPERIDINE HYDROCHLORIDE | Hikma Pharmaceuticals USA Inc. | 15bc51a8-1e24-4d33-9a2f-05a41c29acf0 | 2026-02-27 | Boxed warning, Warnings, Adverse reactions | 861467 861455 |
| Meperidine Hydrochloride | MEPERIDINE HYDROCHLORIDE | Genus Lifesciences Inc. | 792fefda-6cc4-4709-b902-fd9787fc310a | 2026-02-13 | Boxed warning, Warnings, Adverse reactions | 861467 |
| Meperidine Hydrochloride | MEPERIDINE HYDROCHLORIDE | EPIC PHARMA, LLC | fae5cc34-5917-4445-9516-25f97ffca8db | 2025-11-29 | Boxed warning, Warnings, Adverse reactions | 861467 861455 |
| 3C71CD17-EDB3-6EDF-8FF7-C870113EF7F7 | AF5B3E8B-D6DC-4664-89A7-F347D1853ACE | 2007-03-30 | Warnings, Adverse reactions | 3C71CD17-EDB3-6EDF-8FF7-C870113EF7F7 AF5B3E8B-D6DC-4664-89A7-F347D1853ACE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.