NDC 68382-531 – Minocycline hydrochloride
Minocycline Hydrochloride 45 mg/1 · Tablet, Extended Release · Oral
Product NDC68382-531
Product details
- Brand name
- Minocycline hydrochloride
- Generic name
- Minocycline hydrochloride
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203553
- Marketed since
- March 7, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tetracycline-class Drug
Active ingredients
- Minocycline Hydrochloride 45 mg/1
Uses, dosage, side effects and warnings for Minocycline Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-531-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-01) | Mar 7, 2018 |
| 68382-531-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-05) | Mar 7, 2018 |
| 68382-531-06 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-06) | Mar 7, 2018 |
| 68382-531-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-10) | Mar 7, 2018 |
| 68382-531-16 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-531-16) | Mar 7, 2018 |
| 68382-531-30 | 10 BLISTER PACK in 1 CARTON (68382-531-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Mar 7, 2018 |
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- 70771-1154 Minocycline Hydrochloride 65 mg/1 · Tablet, Extended Release · Zydus Lifesciences Limited
- 70771-1157 Minocycline Hydrochloride 105 mg/1 · Tablet, Extended Release · Zydus Lifesciences Limited
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- 70771-1153 Minocycline Hydrochloride 55 mg/1 · Tablet, Extended Release · Zydus Lifesciences Limited