57664-851Level 3
Minocycline Hydrochloride (Minocycline Hydrochloride)
**Product type:** Human Prescription Drug
**Active ingredient:** MINOCYCLINE HYDROCHLORIDE
**Strength:** 50 mg/1
**Dosage form:** Capsule
**Route:** Oral
**Labeler:** Sun Pharmaceutical Industries, Inc.
**Marketing category:** ANDA (ANDA090867)
**Pharmacologic class:** Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
GET
/api/v1/systems/ndc_fda/nodes/57664-851Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.