Methocarbamol

Product NDC: 69036-930
11-digit product format: 690360930
Labeler code: 69036
Product ID: 69036-930_d56deff3-ec7d-49a0-9ad5-bbb109fc4de0
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Methocarbamol
Dosage form: TABLET
Route: ORAL
Labeler: Sallus Laboratories, LLC
Application: ANDA040489
Marketing category: ANDA
Marketing start: 2020-05-15
Marketing end: 0000-00-00
Substance: METHOCARBAMOL
Active strength: 750 mg/1
Pharmacologic classes: Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69036-930-90	2023-11-01	C162847	48780-1	d6a99b39-f4fa-a426-e053-dadaa90af4c2	310b92d3-c788-434f-8011-f6853943c35c
69036-930-90	2022-01-28	C162847	48780-1	d6a99b39-f4fa-a426-e053-dadaa90af4c2	310b92d3-c788-434f-8011-f6853943c35c

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69036-930-90	EA - Each	69036-930	0f5d05f3-d745-4d44-8144-d88acf0b2c6d	1	2020-06-05

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
125OD7737X	METHOCARBAMOL	532-03-6	METHOCARBAMOL

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69036-930-90	69036093090	90 TABLET in 1 BOTTLE (69036-930-90)	90 tablet	2020-05-15	0000-00-00	No	No	Current