Minocycline Hydrochloride 135 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

Minocycline Hydrochloride NDC Family 63629-9210 Minocycline Hydrochloride 135 mg / 1

NDC 11	63629-9210-01
Product NDC	63629-9210
Generic Drug Name	Minocycline Hydrochloride
Brand Name	Minocycline Hydrochloride
Manufacturer	Bryant Ranch Prepack
Strength	135 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	30 Tablet, Film Coated, Extended Release
Package Description	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9210-1)
Active Ingredients	Minocycline Hydrochloride
Marketing Category	ANDA

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NDC snapshot

Minocycline Hydrochloride 135 mg / 1 Tablet is tracked under NDC 63629-9210-01 and rolls up into product family 63629-9210. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 30 Tablet, Film Coated, Extended Release.
Manufacturer: Bryant Ranch Prepack.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyMinocycline Hydrochloride

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Minocycline Hydrochloride 135 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release, NDC 63629-9210-01, is a Bryant Ranch Prepack 135 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated, Extended Release.

NDC search formats

Canonical NDC 11: 63629-9210-01
Digits-only NDC 11: 63629921001
Possible 10-digit display format: 63629-9210-1 (6362992101)

Helpful product links

Search by brand name: Minocycline Hydrochloride
Exact NDC 11: 63629-9210-01
Product family NDC: 63629-9210
VA classification code: AM250
VA classification code description: TETRACYCLINES
CMOP ID: M0698
VUID: 4025712