minocycline hydrochloride
- Product NDC
- 70771-1153
- 11-digit product format
- 707711153
- Labeler code
- 70771
- Product ID
- 70771-1153_5f19958c-a2d2-4ef1-accd-17186e623625
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minocycline hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA203553
- Marketing category
- ANDA
- Marketing start
- 2025-06-12
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 55 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70771-1153-0 | 70771115300 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-0) | | 2025-06-12 | No | No | Historical |
| 70771-1153-1 | 70771115301 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-1) | | 2025-06-12 | No | No | Historical |
| 70771-1153-3 | 70771115303 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-3) | | 2025-06-12 | No | No | Historical |
| 70771-1153-5 | 70771115305 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-5) | | 2025-06-12 | No | No | Historical |
| 70771-1153-7 | 70771115307 | 10 BLISTER PACK in 1 CARTON (70771-1153-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2025-06-12 | No | No | Historical |
| 70771-1153-9 | 70771115309 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1153-9) | | 2025-06-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| minocycline hydrochloride | Zydus Lifesciences Limited | 2025-06-05 | HUMAN PRESCRIPTION DRUG LABEL | 4 |