NDC 72789-529 – Minocycline Hydrochloride
Minocycline Hydrochloride 115 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC72789-529
Product details
- Brand name
- Minocycline Hydrochloride
- Generic name
- Minocycline Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204453
- Marketed since
- September 30, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Tetracycline-class Drug
Active ingredients
- Minocycline Hydrochloride 115 mg/1
Uses, dosage, side effects and warnings for Minocycline Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72789-529-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-529-30) | Sep 10, 2025 |
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