Ranitidine

Manufacturer: Apotex Corp. | Apotex Inc.
Effective date: 2020-03-20
Label type: HUMAN OTC DRUG LABEL
Version: 12
Source: legacy-cache
Hydrated at: 2026-08-01 23:38:15

Label at a glance#

ProductRanitidine

Active ingredientRanitidine Hydrochloride

Label structure10 sections

Indications and uses

relieves heartburn associated with acid indigestion and sour stomach prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Dosage and administration

adults and children 12 years and over: to relieve symptoms, swallow 1 tablet with a glass of water to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn can be used up to twice daily (do not take more than 2 tablets in 24 hours) children under 12 years; ask a doctor

Contacts and useful links#

PhoneLabel contact1-800-706-5575

Label contents#

Full prescribing information#

SPL PRODUCT DATA ELEMENTS SECTION

SPL UNCLASSIFIED SECTION

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Ranitidine 150 mg (as ranitidine hydrochloride, USP 168 mg)

Purpose

OTC - PURPOSE SECTION

Acid reducer

Uses

INDICATIONS & USAGE SECTION

relieves heartburn associated with acid indigestion and sour stomach
prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Warnings

WARNINGS SECTION

Allergy alert: Do not use if you are allergic to ranitidine or other acid reducers.

Do not use

OTC - DO NOT USE SECTION

if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
with other acid reducers
If you have kidney disease, except under the advice and supervision of a doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

had heartburn over 3 months. This may be a sign of a more serious condition.
heartburn with lightheadedness, sweating or dizziness
chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
frequent chest pain
frequent wheezing, particularly with heartburn
unexplained weight loss
nausea or vomiting
stomach pain
kidney disease

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking a prescription drug. Acid reducers may interact with certain prescription drugs.

Stop use and ask a doctor if

OTC - STOP USE SECTION

your heartburn continues or worsens
you need to take this product for more than 14 days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 years and over:
- to relieve symptoms, swallow 1 tablet with a glass of water
- to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn
- can be used up to twice daily (do not take more than 2 tablets in 24 hours)
children under 12 years; ask a doctor

Other information

SPL UNCLASSIFIED SECTION

do not use if printed foil under bottle cap is broken or torn
store at 20°C to 25°C (68°F to 77°F)
avoid excessive heat or humidity
this product is sodium and sugar free

Inactive ingredients

INACTIVE INGREDIENT SECTION

carnauba wax, colloidal silicon dioxide, ferric oxide red, ferric oxide yellow, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, titanium dioxide and vanillin

Questions?

OTC - QUESTIONS SECTION

Call 1-800-706-5575

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Maximum Strength

Ranitidine Tablets USP, 150 mg

Acid Reducer

Prevents & Relieves Heartburn

Associated with Acid Indigestion & Sour Stomach

Distributed by: Apotex Corp. Weston, Florida 33326, USA

ranitidine-150mg-otc-CTN

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Ranitidine Hydrochloride	ACTIVE INGREDIENT	BK76465IHM	6
ranitidine	ACTIVE MOIETY	884KT10YB7	6
Carnauba Wax	INACTIVE INGREDIENT	R12CBM0EIZ	6
Cellulose, Microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	6
Colloidal Silicon Dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	6
Ferric Oxide Red	INACTIVE INGREDIENT	1K09F3G675	6
Ferric Oxide Yellow	INACTIVE INGREDIENT	EX438O2MRT	6
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	6
Magnesium Stearate	INACTIVE INGREDIENT	70097M6I30	6
Polydextrose	INACTIVE INGREDIENT	VH2XOU12IE	6
Titanium Dioxide	INACTIVE INGREDIENT	15FIX9V2JP	6
Vanillin	INACTIVE INGREDIENT	CHI530446X	6

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

Ranitidine
Ranitidine Hydrochloride
CARNAUBA WAX
SILICON DIOXIDE
HYPROMELLOSE, UNSPECIFIED
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYDEXTROSE
TITANIUM DIOXIDE
VANILLIN
FERRIC OXIDE RED
FERRIC OXIDE YELLOW

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60505-2880	60505-2880-7, 60505-2880-0

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Ranitidine Hydrochloride	BK76465IHM	ACTIM
CARNAUBA WAX	R12CBM0EIZ	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
HYPROMELLOSE, UNSPECIFIED	3NXW29V3WO	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
POLYDEXTROSE	VH2XOU12IE	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
VANILLIN	CHI530446X	IACT
FERRIC OXIDE RED	1K09F3G675	IACT
FERRIC OXIDE YELLOW	EX438O2MRT	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 5 · 253 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Ferric Oxide Yellow	FERRIC OXIDE YELLOW	EX438O2MRT	TABLET, COATED / ORAL		1 mg	Exact identifier — unii candidate 20 equally ranked IID candidates
Hypromelloses	HYPROMELLOSE	3NXW29V3WO	GRANULE / ORAL		45 mg	Exact identifier — unii candidate 27 equally ranked IID candidates
Ferric Oxide Red	FERRIC OXIDE RED	1K09F3G675	CREAM / TOPICAL	NA		Exact identifier — unii candidate 21 equally ranked IID candidates
Carnauba Wax	CARNAUBA WAX	R12CBM0EIZ	CAPSULE / ORAL	NA		Exact identifier — unii candidate 11 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	TABLET / BUCCAL	17.5 mg		Exact identifier — unii candidate 39 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	INSERT, EXTENDED RELEASE / OPHTHALMIC	0.4 mg		Exact identifier — unii candidate 40 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	IMPLANT / INTRAVITREAL	NA		Exact identifier — unii candidate 39 equally ranked IID candidates
Ferric Oxide Red	FERRIC OXIDE RED	1K09F3G675	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	3.6 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	POWDER, FOR SUSPENSION / ORAL		120 mg	Exact identifier — unii candidate 39 equally ranked IID candidates
Vanillin	VANILLIN	CHI530446X	TABLET, EXTENDED RELEASE / ORAL	3.4 mg		Exact identifier — unii candidate 15 equally ranked IID candidates
Ferric Oxide Yellow	FERRIC OXIDE YELLOW	EX438O2MRT	CAPSULE, EXTENDED RELEASE / ORAL		7 mg	Exact identifier — unii candidate 20 equally ranked IID candidates
Ferric Oxide Red	FERRIC OXIDE RED	1K09F3G675	TABLET, COATED / ORAL	1 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	CAPSULE, COATED / ORAL		3 mg	Exact identifier — unii candidate 49 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	SOLUTION / ORAL		336 mg	Exact identifier — unii candidate 49 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	TABLET, DELAYED RELEASE PARTICLES / ORAL		170 mg	Exact identifier — unii candidate 49 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	GEL / DENTAL	19 %w/w		Exact identifier — unii candidate 49 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	FILM / BUCCAL		3 mg	Exact identifier — unii candidate 40 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	TROCHE / ORAL		315 mg	Exact identifier — unii candidate 39 equally ranked IID candidates
Carnauba Wax	CARNAUBA WAX	R12CBM0EIZ	TABLET, DELAYED RELEASE / ORAL	230 mg		Exact identifier — unii candidate 11 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	TABLET, DELAYED RELEASE / ORAL		144 mg	Exact identifier — unii candidate 39 equally ranked IID candidates
Hypromelloses	HYPROMELLOSE	3NXW29V3WO	SUSPENSION / OPHTHALMIC	0.5 %w/w		Exact identifier — unii candidate 27 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL	NA		Exact identifier — unii candidate 49 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	POWDER / ORAL		602 mg	Exact identifier — unii candidate 49 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	TABLET / ORAL		980 mg	Exact identifier — unii candidate 39 equally ranked IID candidates
Ferric Oxide Red	FERRIC OXIDE RED	1K09F3G675	CAPSULE / ORAL		5 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
Carnauba Wax	CARNAUBA WAX	R12CBM0EIZ	TABLET, EXTENDED RELEASE / ORAL		2150 mg	Exact identifier — unii candidate 11 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	SUSPENSION / ORAL		400 mg	Exact identifier — unii candidate 49 equally ranked IID candidates
Hypromelloses	HYPROMELLOSE	3NXW29V3WO	TABLET, ORALLY DISINTEGRATING / ORAL		41 mg	Exact identifier — unii candidate 27 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	DROPS / ORAL	NA		Exact identifier — unii candidate 49 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	POWDER, FOR SUSPENSION / ORAL		297 mg	Exact identifier — unii candidate 40 equally ranked IID candidates
Ferric Oxide Red	FERRIC OXIDE RED	1K09F3G675	CAPSULE, COATED / ORAL	0.12 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	LOTION / TOPICAL	NA		Exact identifier — unii candidate 40 equally ranked IID candidates
Hypromelloses	HYPROMELLOSE	3NXW29V3WO	CREAM / TOPICAL	0.1 %w/w		Exact identifier — unii candidate 27 equally ranked IID candidates
Ferric Oxide Red	FERRIC OXIDE RED	1K09F3G675	TABLET, EXTENDED RELEASE / ORAL		7 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	TABLET, EXTENDED RELEASE / ORAL		450 mg	Exact identifier — unii candidate 49 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	DROPS / ORAL	NA		Exact identifier — unii candidate 39 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	SUSPENSION, EXTENDED RELEASE / ORAL		71 mg	Exact identifier — unii candidate 39 equally ranked IID candidates
Cellulose, Microcrystalline	MICROCRYSTALLINE CELLULOSE	OP1R32D61U	TABLET, EXTENDED RELEASE / ORAL		5119 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	SUSPENSION, EXTENDED RELEASE / ORAL		70 mg	Exact identifier — unii candidate 49 equally ranked IID candidates
Ferric Oxide Red	FERRIC OXIDE RED	1K09F3G675	TABLET, CHEWABLE / ORAL		2 mg	Exact identifier — unii candidate 21 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	WAFER / ORAL	66 mg		Exact identifier — unii candidate 39 equally ranked IID candidates
Hypromelloses	HYPROMELLOSE	3NXW29V3WO	SOLUTION / OPHTHALMIC	0.5 %w/v		Exact identifier — unii candidate 27 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	PASTE, DENTIFRICE / DENTAL	0.4 %w/w		Exact identifier — unii candidate 40 equally ranked IID candidates
Ferric Oxide Red	FERRIC OXIDE RED	1K09F3G675	TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL	0.15 mg		Exact identifier — unii candidate 21 equally ranked IID candidates
Carnauba Wax	CARNAUBA WAX	R12CBM0EIZ	OINTMENT / TOPICAL	NA		Exact identifier — unii candidate 11 equally ranked IID candidates
Ferric Oxide Yellow	FERRIC OXIDE YELLOW	EX438O2MRT	TABLET, FILM COATED / ORAL		6 mg	Exact identifier — unii candidate 20 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	INSERT / VAGINAL		8 mg	Exact identifier — unii candidate 49 equally ranked IID candidates
Polydextrose	POLYDEXTROSE	VH2XOU12IE	TABLET, FILM COATED / ORAL		18 mg	Exact identifier — unii candidate 3 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	CAPSULE, DELAYED RELEASE / ORAL		55 mg	Exact identifier — unii candidate 40 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	FILM, EXTENDED RELEASE / TRANSDERMAL	49 mg		Exact identifier — unii candidate 49 equally ranked IID candidates
Ferric Oxide Yellow	FERRIC OXIDE YELLOW	EX438O2MRT	TABLET, DELAYED RELEASE / ORAL		7 mg	Exact identifier — unii candidate 20 equally ranked IID candidates
Cellulose, Microcrystalline	MICROCRYSTALLINE CELLULOSE	OP1R32D61U	TABLET, DELAYED RELEASE / ORAL		2210 mg	Exact identifier — unii candidate 28 equally ranked IID candidates
Hypromelloses	HYPROMELLOSE	3NXW29V3WO	TABLET, COATED / ORAL		58 mg	Exact identifier — unii candidate 27 equally ranked IID candidates
Ferric Oxide Yellow	FERRIC OXIDE YELLOW	EX438O2MRT	POWDER, FOR SUSPENSION / ORAL		3 mg	Exact identifier — unii candidate 20 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	SOAP / TOPICAL	1 %w/w		Exact identifier — unii candidate 40 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	LOZENGE / ORAL		420 mg	Exact identifier — unii candidate 39 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	GUM, CHEWING / BUCCAL		182 mg	Exact identifier — unii candidate 40 equally ranked IID candidates
Magnesium Stearate	MAGNESIUM STEARATE	70097M6I30	TABLET, ORALLY DISINTEGRATING / ORAL		187 mg	Exact identifier — unii candidate 39 equally ranked IID candidates
Titanium Dioxide	TITANIUM DIOXIDE	15FIX9V2JP	SUPPOSITORY / VAGINAL	NA		Exact identifier — unii candidate 40 equally ranked IID candidates
Colloidal Silicon Dioxide	SILICON DIOXIDE	ETJ7Z6XBU4	PASTE / DENTAL	34 %w/w		Exact identifier — unii candidate 49 equally ranked IID candidates

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A200172-001	RANITIDINE HYDROCHLORIDE	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL			2012-05-31

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 44 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2026-10-15 13:18:30	2026-09	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`c2088c7a36db…`
2026-09-14 22:38:34	2026-08	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`ea99ee380514…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A200172-001	RANITIDINE HYDROCHLORIDE	EQ 150MG BASE	TABLET / ORAL	2012-05-31	`3a93d1ddd44b…`

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
89c200d6-4689-189a-1912-65e309c306e8			c816755c-055e-8cbc-9c7a-d794cda2d74b	2020-03-20	Warnings	Exact identifier spl id: 89c200d6-4689-189a-1912-65e309c306e8 spl set id: c816755c-055e-8cbc-9c7a-d794cda2d74b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.