NDC 73377-201 - Minocycline 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
- 73377-201
- Package NDCs from labels
- 73377-201-01, 73377-201-02, 73377-201-03, 73377-201-04, 73377-201-07, 73377-201-08, 73377-201-09
- Manufacturer
- AX Pharmaceutical Corp
- Effective date
- 2024-02-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Minocycline HCl - AX Pharmaceutical Corp | AX Pharmaceutical Corp | 2024-02-05 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73377-201-01 | Minocycline HCl | 10000 g in 1 DRUM | POWDER | 10000 | 5 | |
| 73377-201-02 | Minocycline HCl | 7000 g in 1 DRUM | POWDER | 7000 | 5 | |
| 73377-201-03 | Minocycline HCl | 1000 g in 1 JAR | POWDER | 1000 | 5 | |
| 73377-201-04 | Minocycline HCl | 966 g in 1 JAR | POWDER | 966 | 5 | |
| 73377-201-07 | Minocycline HCl | 100 g in 1 JAR | POWDER | 100 | 5 | |
| 73377-201-08 | Minocycline HCl | 905 g in 1 JAR | POWDER | 905 | 5 | |
| 73377-201-09 | Minocycline HCl | 84 g in 1 JAR | POWDER | 84 | 5 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | NuCare Pharmaceuticals,Inc. | abaacdeb-2433-261a-e053-2995a90ae34e | 2024-07-17 | Warnings, Adverse reactions | 0020414E5U |
| Arestin | MINOCYCLINE HYDROCHLORIDE | OraPharma, Inc. | 8515df41-1936-4f3b-86ba-d2bb2a8441fb | 2024-05-31 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | Advanced Rx Pharmacy of Tennessee, LLC | 192327c5-d2bc-1bd1-e063-6394a90a110b | 2024-05-23 | Warnings, Adverse reactions | 0020414E5U |
| ZILXI | MINOCYCLINE | Journey Medical Corporation | cbffa96e-2446-43cf-ba5e-38c645302afd | 2024-02-09 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | Lupin Pharmaceuticals, Inc. | 3b1e1cf1-ebd2-4aba-a219-9f9939fdb03b | 2023-10-30 | Warnings, Adverse reactions | 0020414E5U |
| AMZEEQ | MINOCYCLINE | Journey Medical Corporation | cc251492-977b-4eb1-a088-a90831324bad | 2023-10-01 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | A-S Medication Solutions | 1229c84c-5627-4992-bb8a-7874b215c543 | 2023-09-17 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | Proficient Rx LP | 4f904969-5af3-461e-b557-d03a1e5c7292 | 2023-05-01 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | Proficient Rx LP | d5fcba91-6aa6-4072-aea5-fb8da65d9aac | 2022-09-01 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | Proficient Rx LP | 49e65b60-ffc9-4ccd-9aec-29a462358d27 | 2022-05-01 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | Strides Pharma Science Limited | d6e136ba-c9b1-4846-ae2a-98a29cb4504d | 2022-03-31 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline hydrochloride | MINOCYCLINE HYDROCHLORIDE | Proficient Rx LP | e6b04358-0f4c-4b21-a7f3-320d1e7bc0b8 | 2021-01-01 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | Proficient Rx LP | d67e4b17-7d44-4d72-9150-420d98cc6db3 | 2019-11-01 | Warnings, Adverse reactions | 0020414E5U |
| Minocycline Hydrochloride | MINOCYCLINE HYDROCHLORIDE | Bryant Ranch Prepack | a84c29a9-21a8-4965-b5a5-37b28e4af5a0 | 2019-06-13 | Warnings, Adverse reactions | 0020414E5U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.