NDC 45802-759-00 - 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
- 45802-759
- Requested NDC
- 45802-759-00
- Package NDCs from labels
- 45802-759-00, 45802-759-30
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2025-12-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Promethazine Hydrochloride - A-S Medication Solutions | A-S Medication Solutions | 2025-12-04 | HUMAN PRESCRIPTION DRUG LABEL |
| Promethazine Hydrochloride Suppositories USP, 25 mg | PD-Rx Pharmaceuticals, Inc. | 2025-10-15 | HUMAN PRESCRIPTION DRUG LABEL |
| ASCORBYL PALMITATE - Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2025-06-07 | HUMAN PRESCRIPTION DRUG LABEL |
| Promethazine Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-01-11 | HUMAN PRESCRIPTION DRUG LABEL |
| Promethazine Hydrochloride - Padagis Israel Pharmaceuticals Ltd | Padagis Israel Pharmaceuticals Ltd | 2023-06-30 | HUMAN PRESCRIPTION DRUG LABEL |
| Promethazine Hydrochloride - Rebel Distributors Corp | Rebel Distributors Corp | 2010-11-11 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 45802-759-00 | Promethazine Hydrochloride | 1 in 1 BLISTER PACK | SUPPOSITORY | 1 | 16 | |
| 45802-759-30 | Promethazine Hydrochloride | 12 in 1 CARTON | SUPPOSITORY | 12 | 16 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 45802-759-00 | EA - Each | 45802-759 | 746555d8-d089-4d29-a28c-93926f76a561 | 1 | 2015-03-03 |
| 45802-759-30 | EA - Each | 45802-759 | 56ac9144-d794-49de-ad4a-1141c6e43e61 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487cd5b9-28f3-392d-e063-6394a90a9ba1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | ATOSAFE CO., Ltd | 487cf27a-d761-6353-e063-6394a90af029 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 487d52d1-8853-bc90-e063-6394a90ab91d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | DONG IL PHARMS CO.,LTD | 487d689d-ebdd-43c3-e063-6294a90af0e2 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487da363-1d01-8cdc-e063-6294a90ac24d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| Berberis Quartz | BERBERIS QUARTZ | Uriel Pharmacy Inc. | 5da48d70-1140-495d-b672-0e55c04196e1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| Promethazine Hydrochloride | PROMETHAZINE HYDROCHLORIDE | Cardinal Health 107, LLC | 7ce351d8-47be-4937-aad2-153208c93b53 | 2026-01-15 | Boxed warning, Warnings, Adverse reactions | R61ZEH7I1I |
| Walgreens Hemorrhoidal | HEMORRHOIDAL RECTAL SUPPOSITORIES | Walgreens | 2dd710ac-ab04-4a24-826f-b5a44d058168 | 2026-01-14 | Warnings | 512OYT1CRR |
| Walgreens Hemorrhoidal | HEMORRHOIDAL RECTAL SUPPOSITORIES | Walgreens | ca98dea5-767d-49a8-887b-d96cad487fc4 | 2026-01-14 | Warnings | 512OYT1CRR |
| Constipation Relief | ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE | Homeocare Laboratories | 62374240-cd14-44e2-9405-5f8996faf047 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Menopause Relief | BARIUM CARBONATE, ATROPA BELLADONNA, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, SILICON DIOXIDE | Homeocare Laboratories | 99b182d5-4102-4b25-85d3-f4be077d753f | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Amber Amethyst | AMBER AMETHYST | Uriel Pharmacy, Inc | 4837e805-a777-c1fa-e063-6294a90ae9c4 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| ECHINACEA | ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS | Marco Pharma International LLC. | 7efadb70-99e4-428b-a8ef-a2797327c6fa | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| RET Stomach 7001 | RET STOMACH | Professional Complementary Health Formulas | 086427e0-599e-4405-a996-d949023f9d90 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Organophosphate Combination 9309 | ORGANOPHOSPHATE COMBINATION | Professional Complementary Health Formulas | f777015f-1df6-4821-af63-543175313aba | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Low Vaccinosis Nosode 4024 | LOW VACCINOSIS NOSODE | Professional Complementary Health Formulas | f347ac8f-ac05-46ef-91a3-9f7e00034768 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| First Chakra (Root) 7301 | FIRST CHAKRA (ROOT) | Professional Complementary Health Formulas | 61eb1bbe-6675-4369-b852-18975e6b08c7 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Second Chakra (Sacral) 7302 | SECOND CHAKRA (SACRAL) | Professional Complementary Health Formulas | ea8a69d3-66fc-4b21-bfdd-c207dd293589 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Silicea 8012 | SILICEA | Professional Complementary Health Formulas | a2a1eae8-24c8-44dd-9b9d-1826fa716433 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Acne Drops 2001 | ACNE DROPS | Professional Complementary Health Formulas | 340fc7dc-2aa4-411f-842b-4ce704671722 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.