Junel, 21 Day - Norethindrone Acetate and Ethinyl Estradiol, 21 Day 20 ug / 1; 1 mg / 1 Tablet 3 Pouch

Reference details for licensed healthcare facility review and verification.

Junel, 21 Day NDC Family 82804-0172 Junel, 21 Day 20 ug / 1; 1 mg / 1

NDC 11	82804-0172-21
Product NDC	82804-0172
Generic Drug Name	Norethindrone Acetate and Ethinyl Estradiol, 21 Day
Brand Name	Junel, 21 Day
Manufacturer	Proficient Rx LP
Strength	20 ug / 1; 1 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	3 Pouch
Package Description	3 POUCH in 1 CARTON (82804-172-21) / 1 BLISTER PACK in 1 POUCH / 21 TABLET in 1 BLISTER PACK
Active Ingredients	Ethinyl Estradiol; Norethindrone Acetate
Marketing Category	ANDA

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NDC snapshot

Norethindrone Acetate and Ethinyl Estradiol, 21 Day 20 ug / 1; 1 mg / 1 Tablet is tracked under NDC 82804-0172-21 and rolls up into product family 82804-0172. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 3 Pouch.
Manufacturer: Proficient Rx LP.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Junel, 21 Day - Norethindrone Acetate and Ethinyl Estradiol, 21 Day 20 ug / 1; 1 mg / 1 Tablet 3 Pouch, NDC 82804-0172-21, is a Proficient Rx LP 20 ug / 1; 1 mg / 1 tablet presentation packaged as 3 Pouch.

NDC search formats

Canonical NDC 11: 82804-0172-21
Digits-only NDC 11: 82804017221
Possible 10-digit display format: 82804-172-21 (8280417221)

Helpful product links

Search by brand name: Junel, 21 Day
Exact NDC 11: 82804-0172-21
Product family NDC: 82804-0172
VA classification code: HS200
VA classification code description: CONTRACEPTIVES,SYSTEMIC
CMOP ID: J0036
VUID: 4033047