71403-102 : Minolira Extended Release 135 mg Oral Tablet
| NDC: | 71403-102 |
| Labeler: | Epi Health, Inc |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Minolira Extended Release |
| Dosage Form: | Oral Tablet |
| Application #: | NDA209269 |
| Rev. Date: |
Appearance:
| Markings: | M3 |
| Shapes: |
Rectangle (4 sides) |
| Colors: |
 White |
| Size (mm): | 20 |
| Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. | |
NDC Package Codes:
- 71403-102-05: 1 BOTTLE IN 1 CARTON (71403‑102‑05) > 5 TABLET IN 1 BOTTLE
- 71403-102-30: 1 BOTTLE IN 1 CARTON (71403‑102‑30) > 30 TABLET IN 1 BOTTLE
Active Ingredients:
- Minocycline Hydrochloride
Dosage Strength:
- 135 mg
Inactive Ingredients:
- Isopropyl Alcohol
- Sodium Stearyl Fumarate
- Talc
- Microcrystalline Cellulose
- Hypromellose 2910 (5 Mpa.s)
- Polyethylene Glycol 400
- Ethylcellulose (10 Mpa.s)
- Hypromellose 2910 (15 Mpa.s)
- Triethyl Citrate
- Hydroxypropyl Cellulose (1600000 Wamw)
- Water /
Pharmaceutical Classes:
- Tetracycline-class Drug [EPC]
- Tetracyclines [CS]
Related Products:
Based on records with the same trade name.- 71403-101 Minolira Extended Release 105 mg Oral Tablet by Epi Health, Inc
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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.