Minocycline Hydrochloride
- Product NDC
- 63629-9210
- 11-digit product format
- 636299210
- Labeler code
- 63629
- Product ID
- 63629-9210_b88e6ee2-70d3-4d6a-bdff-1cafbb2b9daf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204453
- Marketing category
- ANDA
- Marketing start
- 2016-09-30
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 135 mg/1
- Pharmacologic classes
- Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-9210-1 | 63629921001 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9210-1) | 2022-03-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Minocycline Hydrochloride | Bryant Ranch Prepack | 2025-07-03 | HUMAN PRESCRIPTION DRUG LABEL | 106 |