Parathyroid

Product NDC: 55714-6612
Requested package NDC: 55714-6612-1
11-digit product format: 557146612
Labeler code: 55714
Product ID: 55714-6612_b69ddf6a-cff9-4b82-e053-2995a90a6047
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Parathyroid
Dosage form: LIQUID
Route: ORAL
Labeler: Newton Laboratories, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2011-09-01
Marketing end: 0000-00-00
Substance: HUMAN PARATHYROID
Active strength: 15 [hp_X]/mL
NDC exclude flag: No
Listing certified through: 2021-12-31
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	55714-6612	55714-6612-1	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 · 6 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…`
2025-01-20 13:05 UTC · source 2025-01-20	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2020-12-18 03:04 UTC · source 2020-12-17	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`

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
55714-6612-1	2020-12-16	C162847	48780-1	9d75b9cf-e318-f424-e053-dadaa90a57ce	Parathyroid 6612L
55714-6612-1	2020-01-31	C162847	48780-1	9d75b9cf-e318-f424-e053-dadaa90a57ce	Parathyroid 6612L

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Human Parathyroid	ACTIVE INGREDIENT	0SMG1MT0JT	PARATHYROID (PARATHYROID) LIQUID [NEWTON LABORATORIES, INC.]	1
Human Parathyroid	ACTIVE MOIETY	0SMG1MT0JT	PARATHYROID (PARATHYROID) LIQUID [NEWTON LABORATORIES, INC.]	1
Alcohol	INACTIVE INGREDIENT	3K9958V90M	PARATHYROID (PARATHYROID) LIQUID [NEWTON LABORATORIES, INC.]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	PARATHYROID (PARATHYROID) LIQUID [NEWTON LABORATORIES, INC.]	1

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
0SMG1MT0JT	HUMAN PARATHYROID	HUMAN PARATHYROID

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55714-6612-1	55714661201	30 mL in 1 BOTTLE, GLASS (55714-6612-1)	30 ml	2011-09-01	0000-00-00	No	No	Current