Lombrix

Product NDC: 69729-807
11-digit product format: 697290807
Labeler code: 69729
Product ID: 69729-807_3f94048f-d2bd-5a1a-e063-6294a90adf52
Type: HUMAN OTC DRUG
Nonproprietary name: PYRANTEL PAMOATE
Dosage form: TABLET
Route: ORAL
Labeler: OPMX LLC
Application: M024
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-09-24
Substance: PYRANTEL PAMOATE
Active strength: 180 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Lombrix
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
PYRANTEL PAMOATE	180 mg/1

Harmonized Identifiers#

Field, Values table
Field	Values
Unii	81BK194Z5M
Rxcui	199107

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69729-807-10	Lombrix	10 in 1 BLISTER PACK	TABLET	10		1
69729-807-10	Lombrix	1 in 1 CARTON	TABLET	1		1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
199107	pyrantel pamoate 180 MG Oral Tablet	PSN	3f940481-8e75-0bc7-e063-6394a90af1cd	1
199107	pyrantel 180 MG Oral Tablet	SCD	3f940481-8e75-0bc7-e063-6394a90af1cd	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
69729-807-10	69729080710	1 BLISTER PACK in 1 CARTON (69729-807-10) / 10 TABLET in 1 BLISTER PACK	1 blister pack	2025-09-24	No	No	Historical