MINOCYCLINE HYDROCHLORIDE
- Product NDC
- 72162-2575
- 11-digit product format
- 721622575
- Labeler code
- 72162
- Product ID
- 72162-2575_67c910ed-204c-4590-a0eb-e3839f088c86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MINOCYCLINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065156
- Marketing category
- ANDA
- Marketing start
- 2015-04-02
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MINOCYCLINE HYDROCHLORIDE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MINOCYCLINE HYDROCHLORIDE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0020414E5U |
| Rxcui | 207362 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2575-1 | MINOCYCLINE HYDROCHLORIDE | 100 in 1 BOTTLE | TABLET | 100 | | 101 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2575-1 | 72162257501 | 100 TABLET in 1 BOTTLE (72162-2575-1) | 100 tablet | 2025-11-17 | No | No | Current |