cimetidine 200

Product NDC: 0363-0022
11-digit product format: 003630022
Labeler code: 0363
Product ID: 0363-0022_84970421-ebbc-45ad-a5ca-58038d3bf539
Type: HUMAN OTC DRUG
Nonproprietary name: Cimetidine
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Walgreen Company
Application: ANDA075285
Marketing category: ANDA
Marketing start: 2001-03-27
Substance: CIMETIDINE
Active strength: 200 mg/1
Pharmacologic classes: Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Ingredient, Strength table
Ingredient	Strength
CIMETIDINE	200 mg/1

Field, Values table
Field	Values
Unii	80061L1WGD
Rxcui	197505

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
8f48ba86-02a3-4def-9efa-3a8140fd7adf	Product name	2	20250624

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-0022-72	cimetidine 200acid reducer	60 in 1 BOTTLE	TABLET, FILM COATED	60		8
0363-0022-72	cimetidine 200acid reducer	1 in 1 CARTON	TABLET, FILM COATED	1		8

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0363-0022-72	EA - Each	0363-0022	f74dde83-3860-453e-a79c-df6c045c3fea	1	2012-07-24

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CIMETIDINE	ACTIVE INGREDIENT	80061L1WGD	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
CIMETIDINE	ACTIVE MOIETY	80061L1WGD	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	CIMETIDINE ACID REDUCER (CIMETIDINE) TABLET [WALGREEN COMPANY]	2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-0022	CIMETIDINE 200 ACID REDUCER (CIMETIDINE) TABLET, FILM COATED [WALGREEN COMPANY]	8	Current NDC, Legacy NDC, 2 package rows	20250316_7087f4bb-992b-4680-a9a7-452ce74eed2d.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
80061L1WGD	CIMETIDINE	51481-61-9	CIMETIDINE

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
197505	cimetidine 200 MG Oral Tablet	PSN	7087f4bb-992b-4680-a9a7-452ce74eed2d	8
197505	cimetidine 200 MG Oral Tablet	SCD	7087f4bb-992b-4680-a9a7-452ce74eed2d	8

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0363-0022-72	00363002272	1 BOTTLE in 1 CARTON (0363-0022-72) / 60 TABLET, FILM COATED in 1 BOTTLE	1 bottle	2010-04-14	0000-00-00	No	No	Current