Minocycline Hydrochloride
- Product NDC
- 70934-189
- 11-digit product format
- 709340189
- Labeler code
- 70934
- Product ID
- 70934-189_a564359c-524e-bfd5-e053-2995a90ad4c7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA065470
- Marketing category
- ANDA
- Marketing start
- 2018-12-05
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0020414E5U | MINOCYCLINE HYDROCHLORIDE | 13614-98-7 | MINOCYCLINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-189-20 | 70934018920 | 20 CAPSULE in 1 BOTTLE, PLASTIC (70934-189-20) | 20 capsule | 2018-12-05 | 0000-00-00 | No | No | Current |
| 70934-189-60 | 70934018960 | 60 CAPSULE in 1 BOTTLE, PLASTIC (70934-189-60) | 60 capsule | 2020-05-04 | 0000-00-00 | No | No | Current |
| 70934-189-90 | 70934018990 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70934-189-90) | 90 capsule | 2020-05-26 | 0000-00-00 | No | No | Current |