57664-854 : Minocycline 50 mg Oral Tablet, Film Coated
NDC: | 57664-854 |
Labeler: | Sun Pharmaceuticals Industries Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Minocycline |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA090217 |
Rev. Date: |
Appearance:
Markings: | 854 |
Shapes: |
Capsule |
Colors: |
Gray |
Size (mm): | 10 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 57664-854-13: 500 TABLET, FILM COATED IN 1 BOTTLE (57664‑854‑13)
- 57664-854-18: 1000 TABLET, FILM COATED IN 1 BOTTLE (57664‑854‑18)
- 57664-854-85: 50 TABLET, FILM COATED IN 1 BOTTLE (57664‑854‑85)
- 57664-854-88: 100 TABLET, FILM COATED IN 1 BOTTLE (57664‑854‑88)
Active Ingredients:
- Minocycline Hydrochloride
Dosage Strength:
- 50 mg
Inactive Ingredients:
- Lactose Monohydrate
- Cellulose, Microcrystalline
- Povidone
- Sodium Starch Glycolate Type a Potato
- Colloidal Silicon Dioxide
- Magnesium Stearate
- Hypromelloses
- Titanium Dioxide
- Polyethylene Glycols
- Ferrosoferric Oxide
Pharmaceutical Classes:
- Tetracycline-class Drug [EPC]
- Tetracyclines [CS]
Related Products:
Based on records with the same trade name.- 57664-855 Minocycline 75 mg Oral Tablet, Film Coated by Sun Pharmaceuticals Industries Inc.
- 57664-856 Minocycline 100 mg Oral Tablet, Film Coated by Sun Pharmaceuticals Industries Inc.
- 42291-589 Minocycline 50 mg Oral Tablet by Avkare, Inc.
- 42291-591 Minocycline 100 mg Oral Tablet by Avkare, Inc.
- 49884-511 Minocycline (As Minocycline Hydrochloride) 50 mg Oral Tablet by Par Pharmaceutical, Inc.
- 49884-512 Minocycline (As Minocycline Hydrochloride) 75 mg Oral Tablet by Par Pharmaceutical, Inc.
- 49884-513 Minocycline (As Minocycline Hydrochloride) 100 mg Oral Tablet by Par Pharmaceutical, Inc.
- 63629-2228 Minocycline 100 mg Oral Tablet by Bryant Ranch Prepack
- 63629-2229 Minocycline 50 mg Oral Tablet by Bryant Ranch Prepack
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.