Pentazocine Hydrochloride and Acetaminophen is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Gavis Pharmaceuticals, Llc. The primary component is Pentazocine Hydrochloride; Acetaminophen.
Product ID | 43386-670_fc01cb97-4b1c-4f4f-baed-401357b05489 |
NDC | 43386-670 |
Product Type | Human Prescription Drug |
Proprietary Name | Pentazocine Hydrochloride and Acetaminophen |
Generic Name | Pentazocine Hydrochloride And Acetaminophen |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2011-05-11 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA076202 |
Labeler Name | GAVIS Pharmaceuticals, LLC |
Substance Name | PENTAZOCINE HYDROCHLORIDE; ACETAMINOPHEN |
Active Ingredient Strength | 25 mg/1; mg/1 |
Pharm Classes | Competitive Opioid Antagonists [MoA],Partial Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA] |
DEA Schedule | CIV |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2011-05-11 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA076202 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-05-11 |
Inactivation Date | 2019-10-29 |
Ingredient | Strength |
---|---|
PENTAZOCINE HYDROCHLORIDE | 25 mg/1 |
SPL SET ID: | 62a055f3-a58b-446d-9476-af6d36956eaf |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
43386-670 | Pentazocine Hydrochloride and Acetaminophen | Pentazocine Hydrochloride and Acetaminophen |
21695-634 | Pentazocine HCl and Acetaminophen | Pentazocine Hydrochloride and Acetaminophen |