NEWS FROM USA
NEW GENERICS LAUNCHES IN US
|
LAUNCH DATE |
DRUG |
Marketer |
Corresponding RLD |
Annual sales quoted in press release as per IQVIA |
Press Release |
|
09 July 2019 |
Guaifenesin and Pseudoephedrine ER tablets (OTC) |
Dr. Reddy’s laboratories (DRL) |
Mucinex D (RB health) |
$71 Million |
|
|
09 July 2019 |
Imatinib mesylate tablets |
Lupin |
Gleevec (Novartis) |
$548 Million |
NEW 505(b)2 LAUNCHES:
|
LAUNCH DATE |
DRUG |
Marketer |
Brand name |
RLD referred in NDA application |
Press Release |
|
09 July 2019 |
Epinephrine pre-filled syringes |
Sandoz |
Symjepi |
Epipen (Mylan) |
|
|
09 July 2019 |
Levothyroxine sodium injectable solution* |
Fresenius Kabi |
N/A |
Levothyroxine sodium lyophilized powder |
*Comparison between Fresenius’ newly approved solution and previously approved lyophilized product is available here (News 14 April 2019).
505 (b) 2 Approval
|
Approval Date |
Product Name |
NDA Sponsor |
Brand Name |
Prescribing information |
|
08 July 2019 |
Amlodipine benzoate oral suspension |
Silvergate Pharma |
Katerzia |
KEY INFORMATION ON KATERZIA™
- Katerzia™ is the first and only approved Amlodipine oral suspension in the US.
- Indication: for the treatment of hypertension (high blood pressure) in adults and pediatric patients 6 years of age and older and coronary artery disease in adults
- Strength: 1 mg/ml (total volume 150 ml).
- Packaging: HDPE bottle with child resistant cap and tamper-evident seal.
- Storage: refrigerated condition (2°C to 8°C/36°F to 46°F).
- Excipients: citric acid, colloidal silicon dioxide, hypromellose, maltodextrin, polysorbate 80, simethicone, sodium benzoate, sodium besylate, sodium citrate, sodium hydroxide, sucralose, and water.
- Patent application by innovator: US 201890098978
- Full Press release: Link
ANDA APPROVALS
|
Approval Date |
Drug Product |
ANDA Sponsor |
Corresponding RLD |
Number Of Other Approved Generics |
|
03 July 2019 |
Dr Reddys |
Syprine (Aton) |
Five |
|
|
05 July 2019 |
Twi Pharms |
Trilipix (Abbvie) |
Five |
|
|
05 July 2019 |
Glenmark |
RANEXA (GILEAD) |
Six |
|
|
05 July 2019 |
G And W Labs |
Fluoxetine Hydrochloride (Alvogen) |
Seven |
|
|
08 July 2019 |
Annora pharma |
Effexor XR (Wyeth) |
More than 10 |
OTHER NEWS FROM US
Lannett’s distribution agreement with Cediprof for Levothyroxine sodium tablets
- Lannett has entered into a future exclusive supply and distribution agreement for the approved Levothyroxine Sodium Tablets USP of Cediprof, Inc.
- Under the agreement, Lannett will commence U.S. distribution of the product no later than August 1, 2022. Lannett will make an upfront payment of $20 million within the next five business days and will receive a portion of the net profits once it commences distribution of the product.
- Full Press release: Link
Manufacturing Concerns Lead FDA to Pull 31 Apotex ANDAs
- FDA said that it is withdrawing the approval of 31 abbreviated new drug applications (ANDAs) held by Apotex after manufacturing deficiencies were found at two of the company’s plants.
- The two facilities involved, according to FDA, were India-based Apotex Research Private Ltd. and Apotex Pharmachem India Private Ltd.
- Full Article: Link
- Federal register link is available here.
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