16714-109 : Minocycline Hydrochloride 135 mg Oral Tablet, Film Coated, Extended Release
NDC: | 16714-109 |
Labeler: | Northstar Rx LLC |
Product Type: | Human Prescription Drug |
Drug Name: | ![]() |
Dosage Form: | Oral Tablet, Film Coated, Extended Release |
Application #: | ANDA202261 |
Rev. Date: |
Appearance:
Markings: | I;93 |
Shapes: |
Capsule |
Colors: |
![]() |
Size (mm): | 16 |
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:
- 16714-109-01: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (16714‑109‑01)
Active Ingredients:
- Minocycline Hydrochloride
Dosage Strength:
- 135 mg
Inactive Ingredients:
- Silicon Dioxide
- Hypromellose 2208 (4000 Mpa.s)
- Hypromellose 2910 (15 Mpa.s)
- Hypromellose 2910 (6 Mpa.s)
- Lactose Monohydrate
- Magnesium Stearate
- Titanium Dioxide
- Triacetin
- Ferric Oxide Red
- Polyethylene Glycol 3350 /
Pharmaceutical Classes:
- Tetracycline-class Drug [EPC]
- Tetracyclines [CS]
Related Products:
Based on records with the same trade name.- 16714-102 Minocycline Hydrochloride 45 mg Oral Tablet, Film Coated, Extended Release by Northstar Rx LLC
- 16714-103 Minocycline Hydrochloride 55 mg Oral Tablet, Film Coated, Extended Release by Northstar Rx LLC
- 16714-104 Minocycline Hydrochloride 65 mg Oral Tablet, Film Coated, Extended Release by Northstar Rx LLC
- 16714-105 Minocycline Hydrochloride 80 mg Oral Tablet, Film Coated, Extended Release by Northstar Rx LLC
- 16714-106 Minocycline Hydrochloride 90 mg Oral Tablet, Film Coated, Extended Release by Northstar Rx LLC
- 16714-107 Minocycline Hydrochloride 105 mg Oral Tablet, Film Coated, Extended Release by Northstar Rx LLC
- 16714-108 Minocycline Hydrochloride 115 mg Oral Tablet, Film Coated, Extended Release by Northstar Rx LLC
- 0093-2133 Minocycline Hydrochloride 115 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA, Inc.
- 0093-2134 Minocycline Hydrochloride 65 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA, Inc.
- 0093-3165 Minocycline (As Minocycline Hydrochloride) 50 mg Oral Capsule by Teva Pharmaceuticals USA Inc
- 0093-3167 Minocycline (As Minocycline Hydrochloride) 100 mg Oral Capsule by Teva Pharmaceuticals USA Inc
- 0093-7300 Minocycline (As Minocycline Hydrochloride) 75 mg Oral Capsule by Teva Pharmaceuticals USA Inc
- 0093-7741 Minocycline Hydrochloride 55 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA, Inc.
- 0093-7742 Minocycline Hydrochloride 80 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA, Inc.
- 0093-7743 Minocycline Hydrochloride 105 mg Oral Tablet, Film Coated, Extended Release by Teva Pharmaceuticals USA, Inc.
- 0115-1245 Minocycline 45 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories Inc.
- 0115-1246 Minocycline 90 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories Inc.
- 0115-1247 Minocycline 135 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories Inc.
- 0115-7017 Minocycline (As Minocycline Hydrochloride) 50 mg Oral Capsule by Global Pharmaceuticals, Division of Impax Laboratories Inc.
- 0115-7018 Minocycline (As Minocycline Hydrochloride) 100 mg Oral Capsule by Global Pharmaceuticals, Division of Impax Laboratories Inc.
- More related products ...
NDC QR Code
Scan the QR code below to easily reference this data in the future:![NDC 16714-109 QR Code](/images/NDC-QR/16714-109-QR.png)
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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.