Trial Antacid

Product NDC: 35418-310
Requested package NDC: 35418-310-69
11-digit product format: 354180310
Labeler code: 35418
Product ID: 35418-310_f19c5d7f-48e7-d2c6-e053-2995a90a4255
Type: HUMAN OTC DRUG
Nonproprietary name: Calcium Carbonate
Dosage form: TABLET
Route: ORAL
Labeler: Zee Medical Inc
Application: part331
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2012-06-12
Marketing end: 2023-06-01
Substance: CALCIUM CARBONATE
Active strength: 420 mg/1
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	35418-310	35418-310-69	D	Discontinued by firm		2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 16 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2022-08-30 03:57 UTC · source 2022-08-29	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
35418-310-69	2023-01-06	C162847	48780-1	ba0f9c33-28f0-a910-e053-dadaa90a0b85	Drug Facts
35418-310-69	2021-01-29	C162847	48780-1	ba0f9c33-28f0-a910-e053-dadaa90a0b85	Drug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CALCIUM CARBONATE	ACTIVE INGREDIENT	H0G9379FGK	TRIAL ANTACID (CALCIUM CARBONATE) TABLET [ZEE MEDICAL INC]	1
CARBONATE ION	ACTIVE MOIETY	7UJQ5OPE7D	TRIAL ANTACID (CALCIUM CARBONATE) TABLET [ZEE MEDICAL INC]	1
ACACIA	INACTIVE INGREDIENT	5C5403N26O	TRIAL ANTACID (CALCIUM CARBONATE) TABLET [ZEE MEDICAL INC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	TRIAL ANTACID (CALCIUM CARBONATE) TABLET [ZEE MEDICAL INC]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	TRIAL ANTACID (CALCIUM CARBONATE) TABLET [ZEE MEDICAL INC]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	TRIAL ANTACID (CALCIUM CARBONATE) TABLET [ZEE MEDICAL INC]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	TRIAL ANTACID (CALCIUM CARBONATE) TABLET [ZEE MEDICAL INC]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	TRIAL ANTACID (CALCIUM CARBONATE) TABLET [ZEE MEDICAL INC]	1

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
H0G9379FGK	CALCIUM CARBONATE	471-34-1	CALCIUM CARBONATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
35418-310-69	35418031069	500 CARTON in 1 CARTON (35418-310-69) > 50 CARTON in 1 CARTON (35418-310-68) > 125 PACKET in 1 CARTON (35418-310-67) > 2 TABLET in 1 PACKET (35418-310-02)	500 carton	2012-06-12	2023-06-01	No	No	Current