Pituitarum posterium

Product NDC: 0220-4078
11-digit product format: 002204078
Labeler code: 0220
Product ID: 0220-4078_0a21619d-46bd-69a9-e063-6394a90a84ae
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: SUS SCROFA PITUITARY GLAND, POSTERIOR
Dosage form: PELLET
Route: ORAL
Labeler: Boiron
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 1983-03-03
Substance: SUS SCROFA PITUITARY GLAND, POSTERIOR
Active strength: 30 [hp_C]/30[hp_C]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SUS SCROFA PITUITARY GLAND, POSTERIOR	30 [hp_C]/30[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
E8S87O660T	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
875d5270-6c8e-2745-e053-2995a90a3009	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0220-4078-41	2023-11-14	C162847	48780-1	f386c64a-3300-0266-e053-dadaa90a7c1a	Pituitarum posterium 30C
0220-4078-41	2023-01-30	C162847	48780-1	f386c64a-3300-0266-e053-dadaa90a7c1a	Pituitarum posterium 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0220-4078-41	Pituitarum posterium	30 [hp_C] in 1 TUBE	PELLET	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0220-4078	PITUITARUM POSTERIUM (SUS SCROFA PITUITARY GLAND, POSTERIOR ) PELLET [BOIRON]	2	Current NDC, Legacy NDC, 1 package rows	20231115_875d5270-6c8e-2745-e053-2995a90a3009.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pituitarum posterium	SUS SCROFA PITUITARY GLAND, POSTERIOR	Boiron	875d5270-6c8e-2745-e053-2995a90a3009	2023-11-14		Exact identifier ndc (product): 0220-4078

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
E8S87O660T	SUS SCROFA PITUITARY GLAND, POSTERIOR	SUS SCROFA PITUITARY GLAND, POSTERIOR

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0220-4078-41	00220407841	30 [hp_C] in 1 TUBE (0220-4078-41)	1983-03-03	0000-00-00	No	No	Current