NDC 0143-9575-01 - Lidocaine
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
- 0143-9575
- Requested NDC
- 0143-9575-01
- Package NDCs from labels
- 0143-9575-01, 0143-9575-10
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2025-10-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lidocaine - A-S Medication Solutions | A-S Medication Solutions | 2025-10-21 | HUMAN PRESCRIPTION DRUG LABEL |
| LIDOCAINE HCI - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2025-07-09 | HUMAN PRESCRIPTION DRUG LABEL |
| Lidocaine - Hikma Pharmaceuticals USA Inc. | Hikma Pharmaceuticals USA Inc. | 2025-05-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Lidocaine - Medical Purchasing Solutions, LLC | Medical Purchasing Solutions, LLC | 2023-05-16 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0143-9575-01 | Lidocaine | 50 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 50 | 6 | |
| 0143-9575-10 | Lidocaine | 10 in 1 PACKAGE | INJECTION, SOLUTION | 10 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0143-9575 | LIDOCAINE (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION LIDOCAINE (LIDOCAINE HYDROCHLORIDE) INJECTION, SOLUTION [HIKMA PHARMACEUTICALS USA INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250521_5523fdfe-69fd-49a5-b51f-73e2223d49a9.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0143-9575-01 | ML - Milliliter | 0143-9575 | e0e5c666-8931-44d8-b700-5faf7af18880 | 1 | 2017-10-13 |
| 0143-9575-10 | ML - Milliliter | 0143-9575 | 23cc4249-984a-418e-a4b5-e58307ead774 | 1 | 2017-10-13 |
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 |
|---|---|---|---|---|---|---|
| POWERECT Max Power Male Delay | LIDOCAINE HYDROCHLORIDE | SKINS SEXUAL HEALTH LIMITED | 25a1c926-9543-44a7-865e-a4b6e1a40cbe | 2023-11-11 | Warnings | V13007Z41A |
| SKINS DELAY Maximum Strength Lidocaine | LIDOCAINE HYDROCHLORIDE | SKINS SEXUAL HEALTH LIMITED | 172efe5d-28b8-443c-b3f9-429669189081 | 2023-11-11 | Warnings | V13007Z41A |
| LIDOSOLVE PAIN RELIEF | LIDOCAINE HYDROCHLORIDE | HENNIKA HEALTH, LLC | 3a9e4e0c-362d-4e66-bb5f-984fe1c9d4e2 | 2023-11-11 | Warnings | V13007Z41A |
| Uber Numb | LIDOCAINE HYDROCHLORIDE | UBERScientific, LLC | 65a319a6-89d2-44c9-81d5-30327f9948cb | 2023-11-10 | Warnings | V13007Z41A |
| Uber Numb | LIDOCAINE HYDROCHLORIDE | UBERScientific, LLC | 768f3f0e-1add-404f-b869-00a9f35ad34a | 2023-11-10 | Warnings | V13007Z41A |
| Uber Numb Topical Anesthetic | LIDOCAINE HYDROCHLORIDE | UberScientific, LLC | 441c802f-a363-1530-e054-00144ff88e88 | 2023-11-10 | Warnings | V13007Z41A |
| Uber Numb Topical Anesthetic | LIDOCAINE HYDROCHLORIDE | UberScientific, LLC | 4939a547-c94b-3350-e054-00144ff88e88 | 2023-11-10 | Warnings | V13007Z41A |
| CV TOX | COCHLEARIA ARMORACIA, ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, PROPOLIS, GLANDULA SUPRARENALIS BOVINE, THYMUS (SUIS), ARANEA DIADEMA, IPECACUANHA, LYCOPODIUM CLAVATUM, MURIATICUM ACIDUM, NITRICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, SILICEA, EPSTEIN-BARR VIRUS NOSODE, HERPES ZOSTER NOSODE, MORBILLINUM, POLIOMYELITIS NOSODE, HEPATITIS B NOSODE, COXSACKIE B1 NOSODE, CYTOMEGALOVIRUS NOSODE, COXSACKIE B4 NOSODE, EPSTEIN BARR VIRUS NOSODE | BioActive Nutritional, Inc. | 8ef2fb5c-1b24-46a1-8d21-a78ce0a34a87 | 2023-11-07 | Warnings | QTT17582CB |
| Bakers Best Maximum Strength Pain Relief | LIDOCAINE HYDROCHLORIDE, MENTHOL | Baker's Best Health Products, LLC | 9d160ff1-9c23-4a5d-82b3-82c2e1e7d34d | 2023-11-06 | Warnings | V13007Z41A |
| BAKERS BEST Pain Relief with Pure Hemp Seed Oil | LIDOCAINE HYDROCHLORIDE, MENTHOL | BAKER'S BEST HEALTH PRODUCTS, INC. | ae54c234-bfe4-4a74-b293-db7efda7884b | 2023-11-06 | Warnings | V13007Z41A |
| DOCTORS TOUCH Erase The Pain Lidocaine | LIDOCAINE HYDROCHLORIDE | DOCTOR'S CHOICE MEDICAL, LLC | 3dc9947b-8196-4a38-97b4-c2340ee77e0f | 2023-11-06 | Warnings | V13007Z41A |
| RadiaGuard Advanced Radiation Relief | LIDOCAINE HYDROCHLORIDE | SMOOTH SIDE, INC | 21205087-5a2e-41a5-be40-30cba2895408 | 2023-11-06 | Warnings | V13007Z41A |
| SKINS DELAY Climax Control Lidocaine | LIDOCAINE HYDROCHLORIDE | SKINS SEXUAL HEALTH LIMITED | 0db91010-12f7-4f20-b96c-432915720d5a | 2023-11-06 | Warnings | V13007Z41A |
| POWERECT Lidocaine Male Delay | LIDOCAINE HYDROCHLORIDE | SKINS SEXUAL HEALTH LIMITED | 42e0c40f-1efd-45ef-815d-53d193d720eb | 2023-11-06 | Warnings | V13007Z41A |
| WAXUP Numbing | LIDOCAINE HYDROCHLORIDE | CONSTRUSOLUTION, LLC | 4f1645ab-1b19-4d69-99c3-9ea275b01a87 | 2023-11-06 | Warnings | V13007Z41A |
| RAPID PAIN-RELIEF TOPICAL | LIDOCAINE HYDROCHLORIDE, MENTHOL | NORDIC HEALTHY LIVING INC. | a06d6aca-9aa2-4bbe-bf77-4c85f1dd7870 | 2023-11-06 | Warnings | V13007Z41A |
| LidoStat | LIDOCAINE HCL | Clinical Therapeutic Solutions | 1825885b-9141-4515-bb69-a1c4a39fb10d | 2023-11-05 | Warnings | V13007Z41A |
| INSTA RELIEF DM | LIDOCAINE HYDROCHLORIDE, MENTHOL | DM LAB CORP | 6ef66fb9-9f49-409d-9503-175c7555ee9e | 2023-11-05 | Warnings | V13007Z41A |
| SCLERA CARE Topical Anesthetic Gel | LIDOCAINE HYDROCHLORIDE | ScleraCare, LLC | 488ace02-fc0b-4d13-ab89-0e1640e915e5 | 2023-11-05 | Warnings | V13007Z41A |
| Lidocaine Viscous | LIDOCAINE HYDROCHLORIDE | A-S Medication Solutions | 75f2d450-aa2e-4a09-b4f7-4fcbcbf8b205 | 2023-11-01 | Boxed warning, Warnings, Adverse reactions | V13007Z41A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.