Progesterone
- Product NDC
- 43742-0158
- 11-digit product format
- 437420158
- Labeler code
- 43742
- Product ID
- 43742-0158_71ec9f55-0d4b-4c5d-a64d-903a92b67d40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Progesterone
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-09-20
- Marketing end
- 2020-12-22
- Substance
- PROGESTERONE
- Active strength
- 6 [hp_X]/mL
- Pharmacologic classes
- Progesterone [CS],Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record