NDC 65862-883 – Minocycline Hydrochloride
Minocycline Hydrochloride 55 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC65862-883
Product details
- Brand name
- Minocycline Hydrochloride
- Generic name
- Minocycline Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202261
- Marketed since
- August 21, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tetracycline-class Drug
Active ingredients
- Minocycline Hydrochloride 55 mg/1
Uses, dosage, side effects and warnings for Minocycline Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 65862-883-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-01) | Aug 21, 2019 |
| 65862-883-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-05) | Aug 21, 2019 |
| 65862-883-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-30) | Aug 21, 2019 |
| 65862-883-99 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-883-99) | Aug 21, 2019 |
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