MINOCYCLINE HYDROCHLORIDE
- Product NDC
- 61919-845
- 11-digit product format
- 619190845
- Labeler code
- 61919
- Product ID
- 61919-845_8a80a7b8-4069-5d38-e053-2995a90a3f1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MINOCYCLINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA065470
- Marketing category
- ANDA
- Marketing start
- 2019-06-04
- 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
- 2020-12-31
- 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 |
|---|
| 61919-845-30 | 61919084530 | 30 CAPSULE in 1 BOTTLE (61919-845-30) | 30 capsule | 2019-06-04 | 0000-00-00 | No | No | Current |