Annora Pharma OTC
FDA Approved Drugs

Annora Pharma OTC

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

OTC
  • Total Records 6
  • Latest Approval Date Sep 30, 2025
  • Data Source FDA
  • First Approval Date Nov 23, 2018
All
120
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Unclassified
10
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OTC
6
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RX
104
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Company Overview

Company

Annora Pharma OTC

Country

India

Social Profiles

Company Snapshot

Annora Pharma OTC

Sy. No. 261, Annaram Village, Gummadidal Mandal Sangareddy District. Telangana State – 502313

India

www.annorapharma.com/ info@annorapharma.com View on Map
FDA Approved Drug Records ( 6 records )
2021
08 Nov
OTC Application: 215766

Drug Name

FAMOTIDINE

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2021-11-08

215766 / 1

Active Ingredient

FAMOTIDINE

Application Number

215766

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

2021-11-08

Regulatory Status

OTC

2021
08 Nov
OTC Application: 215766

Drug Name

FAMOTIDINE

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2021-11-08

215766 / 2

Active Ingredient

FAMOTIDINE

Application Number

215766

Product Number

2

Dosage Form

-

Strength

20MG

Approval Date

2021-11-08

Regulatory Status

OTC

2018
23 Nov
OTC Application: 210602

Drug Name

IBUPROFEN

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

2018-11-23

210602 / 1

Active Ingredient

IBUPROFEN

Application Number

210602

Product Number

1

Dosage Form

-

Strength

100MG/5ML

Approval Date

2018-11-23

Regulatory Status

OTC

2025
30 Sep
OTC Application: 219102

Drug Name

LEVONORGESTREL

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

2025-09-30

219102 / 1

Active Ingredient

LEVONORGESTREL

Application Number

219102

Product Number

1

Dosage Form

-

Strength

1.5MG

Approval Date

2025-09-30

Regulatory Status

OTC

2021
14 Apr
OTC Application: 214990

Drug Name

POLYETHYLENE GLYCOL 3350

Product Number

1

Dosage Form

-

Strength

17GM/SCOOPFUL

Approval Date

2021-04-14

214990 / 1

Active Ingredient

POLYETHYLENE GLYCOL 3350

Application Number

214990

Product Number

1

Dosage Form

-

Strength

17GM/SCOOPFUL

Approval Date

2021-04-14

Regulatory Status

OTC

2021
14 Apr
OTC Application: 214990

Drug Name

POLYETHYLENE GLYCOL 3350

Product Number

2

Dosage Form

-

Strength

17GM/PACKET

Approval Date

2021-04-14

214990 / 2

Active Ingredient

POLYETHYLENE GLYCOL 3350

Application Number

214990

Product Number

2

Dosage Form

-

Strength

17GM/PACKET

Approval Date

2021-04-14

Regulatory Status

OTC

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Drug Status Breakdown
6 total
  • OTC
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

FAMOTIDINE

Application Number

215766

Product Number

1

Active Ingredient

FAMOTIDINE

Dosage Form

-

Strength

10MG

FDA Approved Drug Data

Approved drug product information

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