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NDC 00904-1987-60 MAPAP 500 mg/1 Details

MAPAP 500 mg/1

MAPAP is a ORAL CAPSULE in the HUMAN OTC DRUG category. It is labeled and distributed by Major Pharmaceuticals. 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: 00904-1987-60
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Acetaminophen

Product Information

NDC	00904-1987
Product ID	0904-1987_a60078f1-193f-9ed2-e053-2995a90abcb3
Associated GPIs	64200010000115
GCN Sequence Number	004473
GCN Sequence Number Description	acetaminophen CAPSULE 500 MG ORAL
HIC3	H3E
HIC3 Description	ANALGESIC/ANTIPYRETICS,NON-SALICYLATE
GCN	16892
HICL Sequence Number	001866
HICL Sequence Number Description	ACETAMINOPHEN
Brand/Generic	Generic
Proprietary Name	MAPAP
Proprietary Name Suffix	Extra Strength
Non-Proprietary Name	Acetaminophen
Product Type	HUMAN OTC DRUG
Dosage Form	CAPSULE
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	ACETAMINOPHEN
Labeler Name	Major Pharmaceuticals
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part343
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00904-1987-60 (00904198760)

Pricing Information
NDC Package Code	0904-1987-60
Billing NDC	00904198760
Package	100 CAPSULE in 1 BOTTLE (0904-1987-60)
Marketing Start Date	1997-12-22
NDC Exclude Flag	N
Price Per Unit	0.03629
Pricing Unit	EA
Effective Date	2023-12-20
NDC Description	MAPAP 500 MG CAPSULE
Pharmacy Type Indicator	C/I
OTC	Y
Explanation Code	4
Classification for Rate Setting	G
As of Date	2024-02-21

This pricing file, entitled the NADAC (National Average Drug Acquisition Cost) files, provide state Medicaid agencies with covered outpatient drug prices by averaging survey invoice prices from retail community pharmacies across the United States. These pharmacies include independent retail community pharmacies and chain pharmacies. The prices are updated on a weekly and monthly basis

Standard Product Labeling (SPL)/Prescribing Information SPL 34a95450-3f04-4de4-9113-73e7bd5724a0 Details

Drug Facts

Active Ingredient (in each banded capsule)

Acetaminophen 500 mg

Purpose

Pain reliever/ Fever reducer

Uses

Temporarily reduces fever and relieves minor aches and pains due to:

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

Warnings

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

more than 4,000 mg of acetaminophen in 24 hours
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 drugs 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 for 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 the 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 capsules every 6 hours while symptoms last
Do not take more than 6 capsules in 24 hours,unless directed by a doctor
Do not take for more than 10 days unless directed by a doctor

children under 12 years: ask a doctor

Other information

store at room temperature

Inactive Ingredients

FD&C Blue #1, FD&C Red #40, Gelatin, Polyvinylpyrrolidone, Pregelatinized Starch, Sodium Starch Glycolate, Stearic Acid and Titanium Dioxide

Questions?

Call: (800) 616-2471

SPL UNCLASSIFIED SECTION

Distributed by: Major® Pharmaceuticals

17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA

Re-order No. 700691 Rev.05/19 M-29 4050-05-19

PRINCIPAL DISPLAY PANEL

Major

NDC 0904-1987-60

EXTRA STRENGTH

Mapap

Acetaminophen 500 mg Each

CAPSULES SAFETY SEALED FOR YOUR PROTECTION

SEE NEW WARNINGS INFORMATION AND DIRECTIONS

ASPIRIN FREE

Strong Pain & Fever Relief

100 CAPSULES

INGREDIENTS AND APPEARANCE

MAPAP EXTRA STRENGTH

acetaminophen capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0904-1987
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Ingredient Name	Strength
Inactive Ingredients
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GELATIN (UNII: 2G86QN327L)
POVIDONE K30 (UNII: U725QWY32X)
STARCH, CORN (UNII: O8232NY3SJ)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white, red	Score	no score
Shape	CAPSULE	Size	22mm
Flavor		Imprint Code	CPC;617
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0904-1987-60	100 in 1 BOTTLE; Type 0: Not a Combination Product	12/22/1997
2	NDC:0904-1987-80	1000 in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2001	04/30/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part343	12/22/1997

Labeler - Major Pharmaceuticals (191427277)

Revised: 5/2020

Document Id: a60078f1-193f-9ed2-e053-2995a90abcb3

Set id: 34a95450-3f04-4de4-9113-73e7bd5724a0

Version: 6

Effective Time: 20200519