Neurontin (Page 9 of 9)

PRINCIPAL DISPLAY PANEL — 470 mL Bottle Label — NDC 0071-2012-44

ALWAYS DISPENSE WITH MEDICATION GUIDE

Pfizer

NDC 0071-2012-44

Neurontin®
(gabapentin)
oral solution

250 mg per 5 mL

470 mL Rx only

PRINCIPAL DISPLAY PANEL -- 470 mL Bottle Label -- NDC 0071-2012-44
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 470 mL Bottle Carton — NDC 0071-2012-44

ALWAYS DISPENSE WITH MEDICATION GUIDE

Pfizer

NDC 0071-2012-44

Neurontin®
(gabapentin)
oral solution

250 mg per 5 mL

470 mL Rx only

PRINCIPAL DISPLAY PANEL -- 470 mL Bottle Carton -- NDC 0071-2012-44
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 470 mL Bottle Label — NDC 0071-2012-47

ALWAYS DISPENSE WITH MEDICATION GUIDE

Pfizer

NDC 0071-2012-47

Neurontin®
(gabapentin)
oral solution

250 mg per 5 mL

470 mL Rx only

PRINCIPAL DISPLAY PANEL -- 470 mL Bottle Label -- NDC 0071-2012-47
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 470 mL Bottle Carton — NDC 0071-2012-47

ALWAYS DISPENSE WITH MEDICATION GUIDE

Pfizer

NDC 0071-2012-47

Neurontin®
(gabapentin)
oral solution

250 mg per 5 mL

470 mL Rx only

PRINCIPAL DISPLAY PANEL -- 470 mL Bottle Carton -- NDC 0071-2012-47
(click image for full-size original)
NEURONTIN gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0071-0803
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GABAPENTIN (GABAPENTIN) GABAPENTIN 100 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE, UNSPECIFIED FORM
STARCH, CORN
TALC
GELATIN, UNSPECIFIED
TITANIUM DIOXIDE
FD&C BLUE NO. 2
Product Characteristics
Color WHITE Score no score
Shape CAPSULE Size 16mm
Flavor Imprint Code PD;Neurontin;100;mg
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0071-0803-24 100 CAPSULE in 1 BOTTLE None
2 NDC:0071-0803-40 50 BLISTER PACK in 1 CARTON contains a BLISTER PACK
2 1 CAPSULE in 1 BLISTER PACK This package is contained within the CARTON (0071-0803-40)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020235 12/30/1993
NEURONTIN gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0071-0805
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GABAPENTIN (GABAPENTIN) GABAPENTIN 300 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE, UNSPECIFIED FORM
STARCH, CORN
TALC
GELATIN, UNSPECIFIED
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
FD&C BLUE NO. 2
Product Characteristics
Color YELLOW Score no score
Shape CAPSULE Size 19mm
Flavor Imprint Code PD;Neurontin;300;mg
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0071-0805-24 100 CAPSULE in 1 BOTTLE None
2 NDC:0071-0805-40 50 BLISTER PACK in 1 CARTON contains a BLISTER PACK
2 1 CAPSULE in 1 BLISTER PACK This package is contained within the CARTON (0071-0805-40)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020235 12/30/1993
NEURONTIN gabapentin capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0071-0806
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GABAPENTIN (GABAPENTIN) GABAPENTIN 400 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE, UNSPECIFIED FORM
STARCH, CORN
TALC
GELATIN, UNSPECIFIED
FERRIC OXIDE RED
TITANIUM DIOXIDE
FERRIC OXIDE YELLOW
FD&C BLUE NO. 2
Product Characteristics
Color ORANGE Score no score
Shape CAPSULE Size 22mm
Flavor Imprint Code PD;Neurontin;400;mg
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0071-0806-24 100 CAPSULE in 1 BOTTLE None
2 NDC:0071-0806-40 50 BLISTER PACK in 1 CARTON contains a BLISTER PACK
2 1 CAPSULE in 1 BLISTER PACK This package is contained within the CARTON (0071-0806-40)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020235 12/30/1993
NEURONTIN gabapentin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0071-0513
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GABAPENTIN (GABAPENTIN) GABAPENTIN 600 mg
Inactive Ingredients
Ingredient Name Strength
POLOXAMER 407
COPOVIDONE K25-31
STARCH, CORN
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
TALC
CANDELILLA WAX
WATER
Product Characteristics
Color WHITE Score 2 pieces
Shape OVAL Size 18mm
Flavor Imprint Code NT;16
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0071-0513-24 100 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020882 10/09/1998
NEURONTIN gabapentin tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0071-0401
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GABAPENTIN (GABAPENTIN) GABAPENTIN 800 mg
Inactive Ingredients
Ingredient Name Strength
POLOXAMER 407
COPOVIDONE K25-31
STARCH, CORN
MAGNESIUM STEARATE
HYDROXYPROPYL CELLULOSE (1600000 WAMW)
TALC
CANDELILLA WAX
WATER
Product Characteristics
Color WHITE Score 2 pieces
Shape OVAL Size 19mm
Flavor Imprint Code NT;26
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0071-0401-24 100 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020882 10/09/1998
NEURONTIN gabapentin solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0071-2012
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GABAPENTIN (GABAPENTIN) GABAPENTIN 250 mg in 5 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
XYLITOL
WATER
Product Characteristics
Color Score
Shape Size
Flavor STRAWBERRY (cool strawberry anise) Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0071-2012-23 470 mL in 1 BOTTLE, GLASS None
2 NDC:0071-2012-44 1 BOTTLE in 1 CARTON contains a BOTTLE
2 470 mL in 1 BOTTLE This package is contained within the CARTON (0071-2012-44)
3 NDC:0071-2012-47 1 BOTTLE, PLASTIC in 1 CARTON contains a BOTTLE, PLASTIC
3 470 mL in 1 BOTTLE, PLASTIC This package is contained within the CARTON (0071-2012-47)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021129 03/02/2000
Labeler — Parke-Davis Div of Pfizer Inc (829076962)

Revised: 07/2022 Parke-Davis Div of Pfizer Inc

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

https://medlibrary.org/lib/rx/meds/neurontin-1/page/9/

Clinical Trials

MedLibrary.org

Medication Sections

RSS Feeds

About

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2023. All Rights Reserved.