NDC 70518-1306-07 - Promethazine Hydrochloride
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
- 70518-1306
- Requested NDC
- 70518-1306-07
- Package NDCs from labels
- 70518-1306-0, 70518-1306-1, 70518-1306-2, 70518-1306-3, 70518-1306-4, 70518-1306-5, 70518-1306-6, 70518-1306-8, 70518-1306-7, 70518-1306-07
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-07-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Promethazine Hydrochloride Tablets USP | REMEDYREPACK INC. | 2026-07-03 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-1306-0 | Promethazine Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | 21 | |
| 70518-1306-1 | Promethazine Hydrochloride | 6 in 1 BOTTLE, PLASTIC | TABLET | 6 | 21 | |
| 70518-1306-2 | Promethazine Hydrochloride | 15 in 1 BOTTLE, PLASTIC | TABLET | 15 | 21 | |
| 70518-1306-3 | Promethazine Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | 21 | |
| 70518-1306-4 | Promethazine Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | 21 | |
| 70518-1306-5 | Promethazine Hydrochloride | 15 in 1 BOTTLE, PLASTIC | TABLET | 15 | 21 | |
| 70518-1306-6 | Promethazine Hydrochloride | 10 in 1 BOTTLE, PLASTIC | TABLET | 10 | 21 | |
| 70518-1306-7 | Promethazine Hydrochloride | 50 in 1 BOX | TABLET | 50 | 21 | |
| 70518-1306-8 | Promethazine Hydrochloride | 1 in 1 POUCH | TABLET | 1 | 21 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-1306 | PROMETHAZINE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 18 | Current NDC, Legacy NDC, 9 package rows | 20250510_9e4e57fa-4ce3-4b7b-be5a-381801ed0386.zip |
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 |
|---|---|---|---|---|---|---|
| PROMETHAZINE HYDROCHLORIDE | PROMETHAZINE HYDROCHLORIDE | Proficient Rx LP | 29a8b172-1bad-40db-8d73-1fe7fb309cff | 2022-04-01 | Warnings, Adverse reactions | 992447 R61ZEH7I1I |
| Promethazine Hydrochloride | PROMETHAZINE HYDROCHLORIDE | Proficient Rx LP | 08bf9fbf-cc21-41a0-9e81-ec498aa64170 | 2019-11-01 | Warnings, Adverse reactions | 992447 R61ZEH7I1I |
| Promethazine Hydrochloride | PROMETHAZINE HYDROCHLORIDE | Actavis Pharma, Inc. | a32255f0-0077-489e-bdc6-869aca8cd434 | 2016-12-01 | Warnings, Adverse reactions | 992475 992447 R61ZEH7I1I |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.