NDC 68180-381 – Minocycline Hydrochloride
Minocycline Hydrochloride 135 mg/1 · Tablet, Extended Release · Oral
Product NDC68180-381
Product details
- Brand name
- Minocycline Hydrochloride
- Generic name
- Minocycline Hydrochloride
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA091424
- Marketed since
- February 14, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tetracycline-class Drug
Active ingredients
- Minocycline Hydrochloride 135 mg/1
Uses, dosage, side effects and warnings for Minocycline Hydrochloride →
Package NDC codes (0)
| Package NDC | Description | Since |
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