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NDC 00363-0336-24 Acetaminophen 650 mg/1 Details

Acetaminophen 650 mg/1

Acetaminophen is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is ACETAMINOPHEN.

MedlinePlus Drug Summary

Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.

Related Packages: 00363-0336-24
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Acetaminophen

Product Information

NDC	00363-0336
Product ID	0363-0336_6116df05-91b5-4f17-b6d7-bc5dcc693b21
Associated GPIs	90859902934120
GCN Sequence Number	022123
GCN Sequence Number Description	acetaminophen TABLET ER 650 MG ORAL
HIC3	H3E
HIC3 Description	ANALGESIC/ANTIPYRETICS,NON-SALICYLATE
GCN	16910
HICL Sequence Number	001866
HICL Sequence Number Description	ACETAMINOPHEN
Brand/Generic	Generic
Proprietary Name	Acetaminophen
Proprietary Name Suffix	n/a
Non-Proprietary Name	Acetaminophen
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	650
Active Ingredient Units	mg/1
Substance Name	ACETAMINOPHEN
Labeler Name	Walgreen Company
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA076200
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00363-0336-24 (00363033624)

Pricing Information	N/A
NDC Package Code	0363-0336-24
Billing NDC	00363033624
Package	24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0363-0336-24)
Marketing Start Date	2002-04-30
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 63be92a2-5093-4971-a193-4c1672350b1a Details

ACTIVE INGREDIENT (IN EACH CAPLET)

Acetaminophen USP, 650 mg

PURPOSE

Pain reliever/fever reducer

USES

•

temporarily relieves minor aches and pains due to:

•: muscular aches
•: backache
•: minor pain of arthritis
•: toothache
•: premenstrual and menstrual cramps
•: headache
•: the common cold

•

temporarily reduces fever

WARNINGS

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

•: more than 6 caplets in 24 hours, which is the maximum daily amount
•: with other drugs containing acetaminophen
•: 3 or more alcoholic drinks every day while using this product
: Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:
•: skin reddening
•: blisters
•: rash
: If a skin reaction occurs, stop use and seek medical help right away.

Do not use

•: with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
•: if you are allergic to acetaminophen or any of the inactive ingredients in this product.

Ask a doctor before use if you have

Liver disease.

Ask a doctor or pharmacist before use if you are

Taking the blood thinning drug warfarin.

Stop use and ask a doctor if

•: pain gets worse or lasts more than 10 days
•: fever gets worse or lasts more than 3 days
•: new symptoms occur
•: redness or swelling is present

These could be signs of a serious condition.

If pregnant or breast-feeding,

Ask a health professional before use.

Keep out of reach of children.

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

DIRECTIONS

•: do not take more than directed (see overdose warning)

adults and children 12 years and over	▪ take 2 caplets every 8 hours with water ▪ swallow whole; do not crush, chew, split or dissolve ▪ do not take more than 6 caplets in 24 hours ▪ do not use for more than 10 days unless directed by a doctor
children under 12 years	▪ do not use

OTHER INFORMATION

•: store at 20 - 25° C (68 - 77° F). Avoid excessive heat 40° C (104° F).
•: see end panel for batch number and expiration date
•: TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.

INACTIVE INGREDIENTS

Croscarmellose sodium, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch, propylene glycol, sodium lauryl sulfate, stearic acid, titanium dioxide

QUESTIONS?

Call 1-800-406-7984

PRINCIPAL DISPLAY PANEL - 24 Caplet Bottle Carton

Walgreens

Compare to Tylenol® 8 HR Muscle

Aches & Pain active ingredient††

NDC 0363-0336-24

8-Hour

Pain Reliever

ACETAMINOPHEN EXTENDED-RELEASE TABLETS USP,

650 mg / PAIN RELIEVER / FEVER REDUCER

MUSCLE PAIN

8 HOUR

CAPLETS

•: Relieves minor muscle pain for up to 8 hours

100

CAPLETS*

(*CAPSULE-SHAPED TABLETS)

ACTUAL SIZE

DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN

spl-apap-walgreens-100-caplet-bottle-carton

INGREDIENTS AND APPEARANCE

ACETAMINOPHEN

acetaminophen tablet, film coated, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-0336
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	650 mg

Ingredient Name	Strength
Inactive Ingredients
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	white	Score	no score
Shape	OVAL (Capsule Shaped)	Size	19mm
Flavor		Imprint Code	cor116
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0363-0336-01	100 in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2002
2	NDC:0363-0336-24	24 in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2002
3	NDC:0363-0336-02	200 in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA076200	04/30/2002

Labeler - Walgreen Company (008965063)

Registrant - Sun Pharmaceutical Industries Inc. (146974886)

Name	Address	ID/FEI	Business Operations
Establishment
Ohm Laboratories Inc.		184769029	MANUFACTURE(0363-0336)

Revised: 9/2019

Document Id: 6116df05-91b5-4f17-b6d7-bc5dcc693b21

Set id: 63be92a2-5093-4971-a193-4c1672350b1a

Version: 5

Effective Time: 20190904