Bolsita, a esta la empece a seguir,y leì las ùltimas motas que no son para nada buenas,ayer se fue de 0,07 y toco 0,094

pero hoy de vuelta a casa,me podes decir que le ves, en cuanto a fundamentos,gracias[/quote]
El arrgue es natural , viene de 0.04 , y di en 0.09 y hoy retome , tengo muchas fichas en esta
Product Pipeline
Programs Under Development
Branded Products (a)
Therapeutic Category
NDA / ANDA
Development Stage (b)
Partnered
ELI-154
Oxycodone CR
Once a day NA
Pain
NDA
Phase III pending
No
ELI-216
Abuse Resistance Product for use with oxycodone or other opioids N/A
Pain
NDA
Phase III pending
No
Undisclosed
Twice a day Undisclosed
Anti-infective
ANDA
Pilot BE study complete
No
Undisclosed
Once a day Undisclosed
Gastrointestinal
ANDA
Pilot BE study complete
Yes
Commercial Products
Commercial
Product
Branded Products (a)
Therapeutic Category
Commercial
Status
Partner
Lodrane®
Once a Day N/A
Allergy
Launched
ECR Pharmaceuticals
Lodrane 24D ®
Once a day N/A
Allergy
Launched
ECR Pharmaceuticals
Methadone Hydrochloride
10 mg tablets Dolophine®
hydrochloride, 10 mg tablets Pain FDA Approved, Launch pending ThePharmaNetwork
Hydromorphone Hydrochloride
8 mg tablets Dilaudid®
8 mg Pain FDA Approved, Launch pending Precision Dose, Inc. / TAGI
Naltrexone Hydrochloride
50 mg ReVia® and Depade® Opioid Receptor Antagonist FDA Approved, Launch pending Precision Dose, Inc. / TAGI
Phentermine HCl 37.5 mg tablets Adipex-P® 37.5 mg Bariatric FDA Approved, Launch pending Precision Dose, Inc. / TAGI
(a) The name of our competitor’s branded product. N/A
(b) Preclinical testing refers to studies done before initiation of any human studies. Pilot Phase I studies for the NDA products are generally preliminary studies done in healthy human subjects to assess the tolerance/safety and pharmacokinetics (PK) of the product. Additional larger studies in humans will be required prior to submission of this product to the FDA for review. Pilot bioequivalence (BE) studies are initial studies done in humans for generic products and are used to assess the likelihood of achieving bioequivalence for generic products. Larger pivotal bioequivalence studies will be required prior to submission of the product for FDA for review.